- Preparation method of glimepiride for anti-diabetes drug, China, , ,
Cas no 93479-97-1 (Glimepiride)
Glimepiride is a third-generation sulfonylurea oral antidiabetic agent used in the management of type 2 diabetes mellitus. It functions by stimulating insulin secretion from pancreatic beta cells through the inhibition of ATP-sensitive potassium channels. Glimepiride exhibits high selectivity for pancreatic sulfonylurea receptors, contributing to its efficacy in glycemic control with a lower risk of extrapancreatic effects. Its extended half-life allows for once-daily dosing, enhancing patient compliance. Additionally, Glimepiride demonstrates a favorable safety profile with a reduced incidence of hypoglycemia compared to earlier sulfonylureas. It is often used as monotherapy or in combination with other antidiabetic agents to achieve optimal blood glucose regulation.
Glimepiride structure
Product Name:Glimepiride
CAS No:93479-97-1
MF:C24H34N4O5S
MW:490.615564823151
MDL:MFCD00878417
CID:61633
PubChem ID:160870906
Update Time:2025-08-05
Glimepiride Chemical and Physical Properties
Names and Identifiers
-
- Glimepiride
- glimepirid
- hoe490
- 1-[[p-[2-(3-ethyl-4-methyl-2-oxo-3-pyrroline-1-carboxamido)ethyl]phenyl]sulfonyl]-3-(trans-4-methylcyclohexyl)urea
- amary
- AMARYL
- Glimperide
- CLIMEPIRIDE
- GliMepiride COS
- Glimpiride
- Grimepride
- trans-3-Ethyl-2,5-dihydro-4-methyl-N-[N-[4-[[[[(4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide
- HOE-490
- Glimepiride impurity
- Amarel
- Glimepiridum
- Glimepirida
- Endial
- Glimepride
- cis-Glimepiride
- Glimepiridum [Latin]
- HOE 490
- Glimepirida [Spanish]
- Glista OD
- 4-ethyl-3-methyl-N-[2-[4-[(4-methylcyclohexyl)carbamoylsulfamoyl]phenyl]ethyl]-5-oxo-2H-pyrrole-1-carboxamide
- 1-((p-(2-(3-Ethyl-4-methyl-2-oxo-3-pyrroline-1-carboxamido)ethyl)phenyl)sulfonyl)-3-(trans-4-methylcyclohexyl)urea
- 24T6XIR2MZ
- 1H-Pyrrole-1-carboxamide, 3-ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-, trans- (ZCI)
- 3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(trans-4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide (ACI)
- Diameprid
- Dibiglim
- Glimax
- Glirid
- GlucoNovax
- Limeral
- trans-3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl] 2-oxo-1H-pyrrole-1-carboxamide
- ZINC 537791
- BRD-K34776109-001-03-4
- BRD-K42693031-001-01-8
- STL451059
- MLS006011260
- gimepiride
- Prestwick1_000651
- CHEMBL1481
- GLIMEPIRIDE [MART.]
- BDBM50237590
- Glimepiride, United States Pharmacopeia (USP) Reference Standard
- DUETACT COMPONENT GLIMEPIRIDE
- boxamide
- CCG-101156
- Glimepiride 100 microg/mL in Acetonitrile
- 684286-46-2
- NSC813217
- HY-B0104
- UNII-6KY687524K
- GLIMEPIRIDE [MI]
- HMS1570C03
- 3-ethyl-4-methyl-N-(4-(N-(((1r,4r)-4-methylcyclohexyl)carbamoyl)sulfamoyl)phenethyl)-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide
- Pharmakon1600-01504915
- Glimepiride, European Pharmacopoeia (EP) Reference Standard
- Sugral
- AC-476
- 1-{[4-(2-{[(3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrol-1-yl)carbonyl]amino}ethyl)phenyl]sulfonyl}-3-(trans-4-methylcyclohexyl)urea
- CHEMBL149223
- AB00513874-08
- 1H-PYRROLE-1-CARBOXAMIDE, 3-ETHYL-2,5-DIHYDRO-4-METHYL-N-(2-(4-(((((CIS-4-METHYLCYCLOHEXYL)AMINO)CARBONYL)AMINO)SULFONYL)PHENYL)ETHYL)-2-OXO-
- 3-ETHYL-4-METHYL-N-(4-(N-((1R,4R)-4-METHYLCYCLOHEXYLCARBAMOYL)SULFAMOYL)PHENETHYL)-2-OXO-2,5-DIHYDRO-1H-PYRROLE-1-CARBOXAMIDE
- 1H-Pyrrole-1-carboxamide, 2,5-dihydro-3-ethyl-4-methyl-N-(2-(4-(((((4-methylcyclohexyl)amino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-oxo-, trans-
- Prestwick0_000651
- HMS3677K06
- SCHEMBL8738802
- Glimepiride Impurity A
- CS-1844
- SR-05000001508-3
- NSC 759809
- s1344
- DTXCID3020675
- Glemax
- GLIMEPIRIDE [WHO-DD]
- GLIMEPIRIDE [USP-RS]
- MFCD00878417
- BSPBio_000681
- 3-Ethyl-4-Methyl-N-[2-(4-{[(Cis-4-Methylcyclohexyl)carbamoyl]sulfamoyl}phenyl)ethyl]-2-Oxo-2,5-Dihydro-1h-Pyrrole-1-Carboxamide
- NC00406
- NCGC00016960-01
- AB00513874-09
- BRD-K34776109-001-15-8
- Ristomycin Monosulfate (90%)
- GLIMEPIRIDE [USAN]
- SPBio_002602
- 1-((4-(2-(((3-ETHYL-4-METHYL-2-OXO-2,3-DIHYDRO-1H-PYRROL-1-YL)CARBONYL)AMINO)ETHYL)PHENYL)SULFONYL)-3-(CIS-4-METHYLCYCLOHEXYL)UREA
- DTXSID5040675
- BRD-K34776109-001-14-1
- Tox21_110713
- SCHEMBL14371714
- BG164507
- SCHEMBL26496475
- Amaryl (TN)
- N'-{[4-(2-{[(3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrol-1-yl)carbonyl]amino}ethyl)phenyl]sulfonyl}-N-(4-methylcyclohexyl)carbamimidic acid
- SMR000466368
- 93479-97-1
- BCP05331
- HMS2235L07
- Glimepiride, >=98% (HPLC), solid
- 3-ethyl-4-methyl-N-{2-[4-({[(4-methylcyclohexyl)carbamoyl]amino}sulfonyl)phenyl]ethyl}-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide
- HMS3654F17
- N-[4-[2-(3-ethyl-4-methyl-2-oxo-3-pyrroline-1-carboxamido)-ethyl]-benzenesulfonyl]-N'-4-methylcyclohexylurea
- trans-1-(4-(2-(3-ethyl-4-Me-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamido)ethyl)phenylsulfonyl)-3-(4-methylcyclohexyl)urea
- BRD-K34776109-001-16-6
- Glimepiride [USAN:USP:INN:BAN]
- MLS000759495
- NCGC00016960-05
- 3-ethyl-4-methyl-N-[2-(4-{[(4-methylcyclohexyl)carbamoyl]sulfamoyl}phenyl)ethyl]-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide
- EN300-19873446
- AB00513874_11
- Solosa
- GLIMEPIRIDE [EP MONOGRAPH]
- NS00004860
- CCRIS 7083
- 3-ethyl-4-methyl-N-[2-(4-{[(trans-4-methylcyclohexyl)carbamoyl]sulfamoyl}phenyl)ethyl]-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide
- C07669
- SR-05000001508-2
- 3-ethyl-4-methyl-N-(4-(N-(((1s,4s)-4-methylcyclohexyl)carbamoyl)sulfamoyl)phenethyl)-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide? (Glimepiride Impurity pound(c)
- Prestwick2_000651
- Oprea1_382896
- STL453194
- Q425027
- NCGC00016960-07
- NCGC00161404-02
- 1H-Pyrrole-1-carboxamide, 3-ethyl-2,5-dihydro-4-methyl-N-(2-(4-(((((4-methylcyclohexyl)amino)carbonyl)amino)sulfonyl)phenyl)ethyl)-2-oxo-, trans-
- 3-Ethyl-4-methyl-N-(4-(N-((rel-(1r,4r)-4-methylcyclohexyl)carbamoyl)sulfamoyl)phenethyl)-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide
- 3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide
- Ristocetin Sulfate; Ristomycin Sulfate
- 1-[[4-[2-[[(3-Ethyl-4-methyl-2-oxo-2,3-dihydro-1H-pyrrol-1-yl)carbonyl]amino]ethyl]phenyl]sulphonyl]-3-(cis-4-methylcyclohexyl)urea (cis-Glimepiride)
- CHEBI:92609
- HMS3372O07
- Glimepiride, British Pharmacopoeia (BP) Reference Standard
- trans-3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(4-methyl cyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide
- Roname
- HMS3269A09
- Glimepiride; 3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(trans-4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl] 2-oxo-1H-pyrrole-1-carboxamide; Amaryl; Glimperide; HOE 490; trans-3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl] 2-oxo-1H-pyrrole-1-carboxamide
- NCGC00371061-02
- CPD000466368
- Tox21_110713_1
- Glymepirid
- NCGC00371061-06
- SCHEMBL16086
- D00593
- 1H-Pyrrole-1-carboxamide, 3-ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(trans- 4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-
- 3-ethyl-4-methyl-N-[2-(4-{[(cis-4-methylcyclohexyl)carbamoyl]sulfamoyl}phenyl)ethyl]-2-oxo-2,5-dihydro-1H-pyrrole-1-car
- GTPL6820
- GLIMEPIRIDE [ORANGE BOOK]
- SR-05000001508-1
- AB00513874
- Q27253874
- HMS2097C03
- Glimepiride for system suitability, European Pharmacopoeia (EP) Reference Standard
- NSC759809
- AB00513874_10
- 6KY687524K
- SCHEMBL14965363
- SR-05000001508
- MLS001076674
- 3-ethyl-4-methyl-N-(4-(N-((1r,4r)-4-methylcyclohexylcarbamoyl)
- HMS3714C03
- BCP9000728
- NCGC00016960-04
- BPBio1_000751
- Trans-3-Ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide
- Z1501475009
- GLIMEPIRIDE [VANDF]
- Glimepiride for system suitability
- 3-ethyl-4-methyl-N-[2-(4-{[(cis-4-methylcyclohexyl)carbamoyl]sulfamoyl}phenyl)ethyl]-2-oxo-2,5-dihydro-1H-pyrrole-1-car boxamide
- UNII-24T6XIR2MZ
- Glimepiride,(S)
- GLIMEPIRIDE IMPURITY A [EP IMPURITY]
- CHEBI:5383
- SL-NH2 Trifluoroacetic Acid Salt (1:2)
- GLIMEPIRIDE [INN]
- GLIMEPIRIDE [USP IMPURITY]
- MLS001401419
- 261361-60-8
- AB00513874-06
- 3-ethyl-4-methyl-2-oxo-N-(2-{4-[({[(1r,4r)-4-methylcyclohexyl]carbamoyl}amino)sulfonyl]phenyl}ethyl)-2,5-dihydro-1H-pyrrole-1-carboxamide
- G0395
- Glimepiride- Bio-X
- HMS2052L03
- AKOS015894919
- AKOS015969663
- Amaryl, Glista OD
- Q-201158
- NSC-759809
- NCGC00181757-01
- Niddaryl
- Prestwick3_000651
- SCHEMBL16084
- 3-ethyl-4-methyl-n-(4-(n-((1r,4r)-4-methylcyclohexylcarbamoyl)sulfamoyl)phenethyl)-2-oxo-2,5-dihydro
- MLS003915622
- NCGC00161404-01
- GLIMEPIRIDE [EMA EPAR]
- Glimepiride, cis-
- HMS3394L03
- GLIMEPIRIDE [USP MONOGRAPH]
- sulfamoyl)phenethyl)-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide
- Glimer
- SW196369-4
- AB07644
- Glorion
- GLIMEPIRIDE CIS-ISOMER
- GLIMEPIRIDE [JAN]
- Glimepiride (JP18/USP/INN)
- NCGC00016960-02
- BRN 5365754
- HMS2090K18
- CAS-93479-97-1
- HMS3413K06
- KS-5238
- SMR001550123
- NCGC00016960-03
- DB00222
- DTXSID20861130
- CS-0165191
- NSC-813217
-
- MDL: MFCD00878417
- Inchi: 1S/C24H34N4O5S/c1-4-21-17(3)15-28(22(21)29)24(31)25-14-13-18-7-11-20(12-8-18)34(32,33)27-23(30)26-19-9-5-16(2)6-10-19/h7-8,11-12,16,19H,4-6,9-10,13-15H2,1-3H3,(H,25,31)(H2,26,27,30)/t16-,19-
- InChI Key: WIGIZIANZCJQQY-RUCARUNLSA-N
- SMILES: C(N1CC(C)=C(CC)C1=O)(=O)NCCC1C=CC(S(=O)(=O)NC(=O)N[C@@H]2CC[C@@H](C)CC2)=CC=1
- BRN: 5365754
Computed Properties
- Exact Mass: 490.22500
- Monoisotopic Mass: 490.224991
- Isotope Atom Count: 0
- Hydrogen Bond Donor Count: 3
- Hydrogen Bond Acceptor Count: 5
- Heavy Atom Count: 34
- Rotatable Bond Count: 7
- Complexity: 895
- Covalently-Bonded Unit Count: 1
- Defined Atom Stereocenter Count: 0
- Undefined Atom Stereocenter Count : 0
- Defined Bond Stereocenter Count: 0
- Undefined Bond Stereocenter Count: 0
- Topological Polar Surface Area: 133
- Surface Charge: 0
- Tautomer Count: 6
- XLogP3: 3.9
Experimental Properties
- Color/Form: Powder
- Density: 1.29
- Melting Point: 202.0 to 206.0 deg-C
- Boiling Point: No data available
- Flash Point: No data available
- Refractive Index: 1.599
- Solubility: DMSO: >10?mg/mL
- PSA: 133.06000
- LogP: 5.26540
- Merck: 4440
- Solubility: Not determined
Glimepiride Security Information
-
Symbol:
- Prompt:warning
- Signal Word:Warning
- Hazard Statement: H361
- Warning Statement: P280
- Hazardous Material transportation number:NONH for all modes of transport
- WGK Germany:3
- Hazard Category Code: R21: harmful in contact with skin. R46: may cause genetic damage. R62: risk of weakening reproductive capacity. R63: may harm unborn infants. R36/38: irritating to eyes and skin.
- Safety Instruction: S25-S26-S36/37-S53
- RTECS:UX9363950
-
Hazardous Material Identification:
- Storage Condition:Powder -20°C 3 years ? 4°C 2 years In solvent -80°C 6 months ? -20°C 1 month
- Risk Phrases:R21
Glimepiride Customs Data
- HS CODE:2935009090
- Customs Data:
China Customs Code:
2935009090Overview:
2935009090 Other sulphonates(Acyl)amine. VAT:17.0% Tax refund rate:9.0% Regulatory conditions:nothing MFN tariff:6.5% general tariff:35.0%
Declaration elements:
Product Name, component content, use to
Summary:
2935009090 other sulphonamides VAT:17.0% Tax rebate rate:9.0% Supervision conditions:none MFN tariff:6.5% General tariff:35.0%
Glimepiride Pricemore >>
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Glimepiride Production Method
Production Method 1
Reaction Conditions
1.1 Reagents: Triethylamine Solvents: Dichloromethane ; 7 h, rt
Reference
Production Method 2
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Tetrahydrofuran ; 1 - 2 h, rt → 65 °C
1.2 Solvents: Toluene ; 10 - 12 h, 60 - 65 °C; cooled
1.3 Reagents: Ammonia Solvents: Methanol ; pH 10 - 12
1.4 Reagents: Acetic acid ; pH 5.5 - 6.0, 25 - 30 °C
1.2 Solvents: Toluene ; 10 - 12 h, 60 - 65 °C; cooled
1.3 Reagents: Ammonia Solvents: Methanol ; pH 10 - 12
1.4 Reagents: Acetic acid ; pH 5.5 - 6.0, 25 - 30 °C
Reference
- A process for purification of glimepiride, India, , ,
Production Method 3
Reaction Conditions
1.1 Reagents: Sodium methoxide Solvents: Dimethyl sulfoxide
1.2 Reagents: Water
1.2 Reagents: Water
Reference
- Improved process for the preparation of benzenesulfonylureas used as second-generation oral hypoglycemic agents, World Intellectual Property Organization, , ,
Production Method 4
Reaction Conditions
1.1 Solvents: Toluene
Reference
- Studies on synthetic process of glimepiride, new hypoglycemic agentDeng, Yong; Zhong, Yuguo; Tang, Weigao; Zhong, Zhicheng, Zhongguo Yaowu Huaxue Zazhi, 2000, 10(2), 134-137
Production Method 5
Reaction Conditions
1.1 Solvents: Toluene ; rt
1.2 rt → reflux; 4 h, reflux; reflux → 15 °C
1.2 rt → reflux; 4 h, reflux; reflux → 15 °C
Reference
- Process for preparing glimepiride and corresponding intermediate, Czech Republic, , ,
Production Method 6
Reaction Conditions
1.1 Reagents: Triethylamine , Ethyl chloroformate Solvents: Dichloromethane ; 2 h, 20 - 25 °C
1.2 Reagents: Acetic acid Solvents: Water ; pH 4 - 4.2; 30 min
1.3 Reagents: 4-(Dimethylamino)pyridine Solvents: Toluene ; rt → reflux; 3 h, reflux; reflux → 30 °C; 3 h, 25 - 30 °C
1.2 Reagents: Acetic acid Solvents: Water ; pH 4 - 4.2; 30 min
1.3 Reagents: 4-(Dimethylamino)pyridine Solvents: Toluene ; rt → reflux; 3 h, reflux; reflux → 30 °C; 3 h, 25 - 30 °C
Reference
- An improved process for the preparation of N-{2-[4-(aminosulfonyl)phenyl]ethyl}-3-ethyl-4-methyl-2-oxo-2,5-dihydro-1H-pyrrole-1-carboxamide, a key intermediate in the synthesis of glimepiride, India, , ,
Production Method 7
Reaction Conditions
1.1 Reagents: Diisopropylethylamine Solvents: Dimethylformamide ; 3 h, rt → 25 °C
1.2 Solvents: Dimethylformamide ; overnight, heated
1.2 Solvents: Dimethylformamide ; overnight, heated
Reference
- Preparation method of glimepiride, China, , ,
Production Method 8
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetonitrile ; rt → 60 °C
1.2 6 h, 50 - 60 °C
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 1 - 2, 20 - 25 °C
1.2 6 h, 50 - 60 °C
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 1 - 2, 20 - 25 °C
Reference
- Synthetic preparation of glimepiride bulk drug, China, , ,
Production Method 9
Reaction Conditions
1.1 Solvents: tert-Butyl methyl ether
1.2 Solvents: Toluene , Cyclohexanone , tert-Butyl methyl ether ; 10 h, 30 °C
1.2 Solvents: Toluene , Cyclohexanone , tert-Butyl methyl ether ; 10 h, 30 °C
Reference
- Method for preparing hypoglycemic drug glimepiride, China, , ,
Production Method 10
Reaction Conditions
1.1 Reagents: 4-(Dimethylamino)pyridine Solvents: Toluene ; rt → reflux
Reference
- Method for the manufacture of compounds related to the class of substituted sulfonyl urea antidiabetics, European Patent Organization, , ,
Production Method 11
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetone , Methyl ethyl ketone ; 30 min, rt → reflux
1.2 5 - 6 h, reflux
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 6
1.2 5 - 6 h, reflux
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 6
Reference
- Preparation of glimepiride, China, , ,
Production Method 12
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetone ; 1 h, 55 - 60 °C
1.2 Solvents: Toluene ; 12 h, reflux
1.3 Reagents: Acetic acid Solvents: Water ; pH 5.5 - 6, 20 - 25 °C
1.2 Solvents: Toluene ; 12 h, reflux
1.3 Reagents: Acetic acid Solvents: Water ; pH 5.5 - 6, 20 - 25 °C
Reference
- A novel process for preparation of substantially pure glimepiride, World Intellectual Property Organization, , ,
Production Method 13
Reaction Conditions
1.1 Reagents: 1,8-Diazabicyclo[5.4.0]undec-7-ene Solvents: Acetonitrile ; 5 h, reflux
Reference
- An Efficient and Practical Process for the Synthesis of GlimepirideTanwar, Dinesh Kumar; Surendrabhai, Vaghela Ravikumar; Gill, Manjinder Singh, Synlett, 2017, 28(18), 2495-2498
Production Method 14
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetone ; 6 h, reflux
1.2 6 h, reflux; reflux → rt
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 2
1.2 6 h, reflux; reflux → rt
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 2
Reference
- studies on the preparation of glimepirideLiu, Sheng-gao, Shandong Huagong, 2009, 38(6), 14-15
Production Method 15
Reaction Conditions
1.1 Reagents: Potassium carbonate Solvents: Acetone ; 6 h, reflux
1.2 8 h, reflux; reflux → rt
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 1 - 2
1.2 8 h, reflux; reflux → rt
1.3 Reagents: Hydrochloric acid Solvents: Water ; pH 1 - 2
Reference
- Synthesis of 3-ethyl-2,5-dihydro-4-methyl-N-[2-[4-[[[[(trans-4-methylcyclohexyl)amino]carbonyl]amino]sulfonyl]phenyl]ethyl]-2-oxo-1H-pyrrole-1-carboxamide (glimepiride)Liu, Zhanke; Yang, Xinwu; Lu, Qihui; Wang, Xiaoguang; Liu, Zhiling, Jingxi Huagong Zhongjianti, 2006, 36(3), 16-18
Production Method 16
Reaction Conditions
1.1 Reagents: Sodium hydroxide , Zinc chloride Solvents: Dimethylformamide , Water ; pH 6.5 - 8, rt; 3 h, 80 °C
Reference
- Synthesis, physico-chemical and antidiabetic studies of zinc complex of glimepiride, an oral hypoglycemic agentJacob, George, Oriental Journal of Chemistry, 2013, 29(4), 1351-1358
Glimepiride Raw materials
- 2,2-dimethylpropanoic acid
- trans-4-Methycyclohexyl Isocyanate
- 4-2-(3-Ethyl-4-methyl-2-oxo-3-pyrrolin-1-yl)carboxamidoethylbenzenesulfonamide
- Glimepiride
- 4-2-(3-Ethyl-2,5-dihydro-4-methyl-2-oxo-1H-pyrrol-1-yl)carbonylaminoethylphenylsulfonylcarbamic Acid Ethyl Ester
- Phenyl N-(trans-4-methylcyclohexyl)carbamate
- N,N'-Carbonyldiimidazole
- trans-4-Methylcyclohexanamine
- Carbamic acid, (trans-4-methylcyclohexyl)-, 4-nitrophenyl ester
Glimepiride Preparation Products
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Amadis Chemical Company Limited
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(CAS:93479-97-1)Glimepiride
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Stock Status:in Stock
Quantity:25g
Purity:99%
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Tiancheng Chemical (Jiangsu) Co., Ltd
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(CAS:93479-97-1)格列吡咯
Order Number:LE25877165;LE12400
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Quantity:25KG,200KG,1000KG
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Suzhou Senfeida Chemical Co., Ltd
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(CAS:93479-97-1)Glimepiride
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Quantity:200kg
Purity:99.9%
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Zhengzhou Baoyu Pharmaceutical Co., Ltd.
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(CAS:93479-97-1)Glimepiride
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Quantity:5KG/1KG/25KG/100KG
Purity:99% HPLC
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Glimepiride Related Literature
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1. An amorphous lanthanum–iridium solid solution with an open structure for efficient water splitting?Wei Sun,Chenglong Ma,Xinlong Tian,Jianjun Liao,Ji Yang,Chengjun Ge,Weiwei Huang J. Mater. Chem. A, 2020,8, 12518-12525
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Haitao Li,Yu Pan,Zhizhi Wang,Shan Chen,Ruixin Guo,Jianqiu Chen RSC Adv., 2015,5, 100775-100782
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4. An all-solid-state imprinted polymer-based potentiometric sensor for determination of bisphenol S?Rongning Liang,Tanji Yin,Ruiqing Yao,Wei Qin RSC Adv., 2016,6, 73308-73312
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S. Amaresh,K. Karthikeyan,K. J. Kim,Y. S. Lee RSC Adv., 2014,4, 23107-23115