Production Method 1

930-37-0

93372-65-7

Reaction Conditions

1.1 Reagents: Ammonium chloride ,  Sodium azide Solvents: Dimethylformamide ,  Water ;  rt → 80 °C; 3 h, 80 °C
1.2 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol ;  5 h, rt

Reference

Short-acting benzodiazepine derivatives, preparation method therefor, and use thereof

, China, , ,

Production Method 2

93372-65-7

Reaction Conditions

Reference

New non-ionic iodized x-ray contrast agents, method for preparing them, and galenical compositions containing them

, World Intellectual Property Organization, , ,

Production Method 3

168431-71-8

93372-65-7

Reaction Conditions

1.1 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol ;  48 h, 650 psi, rt → 70 °C

Reference

Reinventing Design Principles for Developing Low-Viscosity Carbon Dioxide-Binding Organic Liquids for Flue Gas Clean Up

Malhotra, Deepika ; Koech, Phillip K. ; Heldebrant, David J. ; Cantu, David C.; Zheng, Feng; et al, ChemSusChem, 2017, 10(3), 636-642

Production Method 4

930-37-0

93372-65-7

Reaction Conditions

1.1 Reagents: Ammonium chloride ,  Sodium azide Solvents: Dimethylformamide ,  Water ;  rt → 80 °C; 3 h, 80 °C
1.2 Reagents: Hydrogen Catalysts: Palladium Solvents: Methanol ;  5 h, rt

Reference

Benzodiazepine compound-containing injectable composition and preparation method therefor

, World Intellectual Property Organization, , ,

Production Method 5

930-37-0

93372-65-7

Reaction Conditions

1.1 Reagents: Ammonium hydroxide Solvents: Water ;  20 °C; 20 °C → 40 °C; 24 h, rt

Reference

Synthesis of thiocarbamides based on 1-amino-3-methoxy-2-propanol

Mammadova, A. R.; Maharramov, A. M.; Aliyev, S. G.; Allakhverdiyev, M. A., Azerbaidzhanskii Khimicheskii Zhurnal, 2009, (3), 171-173

Production Method 6

930-37-0

93372-65-7

Reaction Conditions

1.1 Reagents: Ammonia Solvents: Methanol ;  18 h, 20 °C

Reference

Preparation of heterocyclyl compounds for restoring mutant p53 function

, World Intellectual Property Organization, , ,

Production Method 7

93372-65-7

Reaction Conditions

Reference

Heteroarylalkyne compounds for targeting mutant of p53 and their preparation

, World Intellectual Property Organization, , ,

1-Amino-3-methoxypropan-2-ol Raw materials

• 1-azido-3-methoxypropan-2-ol
• 2-(Methoxymethyl)oxirane

1-Amino-3-methoxypropan-2-ol Preparation Products

• 1-Amino-3-methoxypropan-2-ol (93372-65-7)

• 1. An approach to 7-aza-1-phosphanorbornane complexes: strain promoted rearrangement of 1-iminylphosphirane complexes and cycloaddition with olefins?
  Yang Xu,Min Wang,Donghui Wei,Rongqiang Tian,Zheng Duan,Fran?ois Mathey Dalton Trans., 2019,48, 5523-5526
• 2. Alternative mixtures to R-600a. Theoretical assessment and experimental energy evaluation of binary mixtures in a commercial cooler: Mélanges alternatifs au R-600a. évaluation théorique et évaluation énergétique expérimentale de mélanges binaires dans un refroidisseur commercial.
  DanielCalleja-Anta,DanielSánchez,LauraNebot-Andres,RamónCabello,RodrigoLlopis
• 3. An integrated droplet-digital microfluidic system for on-demand droplet creation, mixing, incubation, and sorting?
  Lab Chip, 2019,19, 524-535
• 4. An approach towards the synthesis of novel fused nitrogen tricyclic heterocyclic scaffolds via GBB reaction?
  Sandip Gangadhar Balwe,Yeon Tae Jeong Org. Biomol. Chem., 2018,16, 1287-1296
• 5. Alternative synthesis of the anti-baldness compound RU58841?
  RSC Adv., 2014,4, 14143-14148

• Solvents and Organic Chemicals Organic Compounds Organic nitrogen compounds Organonitrogen compounds Amines Alkanolamines

• 83585-56-2(2-Aminomethyl-15-crown-5)
• 94616-61-2(1,4,7,10-Tetraoxacyclododecane-2-methanamine)
• 83585-61-9(2-Aminomethyl-18-crown-6)
• 3141-83-1(1-Amino-3-isopropoxy-propan-2-ol)
• 114012-79-2(1-amino-3-(2-hydroxyethoxy)propan-2-ol)
• 35152-18-2(1-Amino-3-ethoxypropan-2-ol)
• 214190-74-6(1-Amino-3-(3-aminopropoxy)propan-2-OL)
• 163340-45-2(3-(3-Amino-2-hydroxypropoxy)-1,2-propanediol)
• 13861-28-4(2-Propanol, 1,1'-[1,4-butanediylbis(oxy)]bis[3-amino-)
• 4454-09-5(2-PROPANOL, 1,1'-[1,2-ETHANEDIYLBIS(OXY)]BIS[3-AMINO-)