Production Method 1

885278-42-2

946427-77-6

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Acetonitrile ;  15 h, rt

Reference

Preparation of isoxazolylmethoxyheterocyclylarenecarboxylates and related compounds as farnesoid X receptor (FXR) agonists for treatment of dyslipidemia.

, World Intellectual Property Organization, , ,

Production Method 2

885278-42-2

946427-77-6

Reaction Conditions

Reference

Preparation of 3-phenylisoxazole derivatives for treatment of dyslipidemia

, World Intellectual Property Organization, , ,

Production Method 3

660823-36-9

946427-77-6

Reaction Conditions

1.1 Reagents: Sodium hydride Solvents: Tetrahydrofuran ;  30 min, 0 °C
1.2 0 °C; 1 h, 0 °C

Reference

Preparation of indazoles for treating flaviviridae virus infection

, World Intellectual Property Organization, , ,

Production Method 4

885278-42-2

946427-77-6

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Acetonitrile ;  15 h, rt

Reference

Preparation of substituted methoxyphenylcyclopropane derivatives for use as NR1 H4 receptor agonists useful in treatment and prophylaxis of FXR-mediated diseases

, World Intellectual Property Organization, , ,

Production Method 5

885278-42-2

946427-77-6

Reaction Conditions

1.1 Reagents: Potassium carbonate Solvents: Dimethylformamide ,  Acetonitrile ;  20 - 25 °C; 0 °C; 16 h, 20 - 25 °C

Reference

Preparation of indazole derivatives for use as pesticides

, World Intellectual Property Organization, , ,

Production Method 6

885278-42-2

946427-77-6

Reaction Conditions

1.1 Reagents: Potassium carbonate ;  overnight, rt

Reference

Bicyclic heteroaryls as kinase inhibitors and their preparation

, World Intellectual Property Organization, , ,

Production Method 7

885278-42-2

946427-77-6

Reaction Conditions

Reference

Aryltriazole derivatives as FXR modulators and their preparation, pharmaceutical compositions and use in the treatment of dyslipidemia and related diseases

, World Intellectual Property Organization, , ,

Production Method 8

946427-77-6

Reaction Conditions

Reference

Preparation of bifunctionalized compounds as coronavirus non-structural protein 3 degrading compounds

, World Intellectual Property Organization, , ,

Production Method 9

946427-77-6

Reaction Conditions

Reference

Arylpyrazole derivatives as FXR agonists and their preparation, pharmaceutical compositions and use in the treatment of dyslipidemia and related diseases

, World Intellectual Property Organization, , ,

Methyl 6-bromo-1-methyl-1H-indazole-3-carboxylate Raw materials

• 6-Bromo-1H-indazole-3-carboxylic acid
• Methyl 6-bromo-1H-indazole-3-carboxylate

Methyl 6-bromo-1-methyl-1H-indazole-3-carboxylate Preparation Products

• Methyl 6-bromo-1-methyl-1H-indazole-3-carboxylate (946427-77-6)

• 1. Exceptional activity of sub-nm Pt clusters on CdS for photocatalytic hydrogen production: a combined experimental and first-principles study?
  Qiyuan Wu,Shangmin Xiong,Peichuan Shen,Shen Zhao,Alexander Orlov Catal. Sci. Technol., 2015,5, 2059-2064
• 2. Excitation dependent recombination studies on SnO2/TiO2 electrospun nanofibers?
  Veluru Jagadeesh babu,Sesha Vempati RSC Adv., 2015,5, 66367-66375
• 3. Dissociative electron attachment to HGaF4 Lewis–Br?nsted superacid
  Marcin Czapla,Jack Simons Phys. Chem. Chem. Phys., 2018,20, 21739-21745
• 4. Enantiomeric two-fold interpenetrated 3D zinc(ii) coordination networks as a catalytic platform: significant difference between water within the cage and trace water in transesterification?
  Eunkyung Choi,Minjoo Ryu,Haeri Lee,Ok-Sang Jung Dalton Trans., 2017,46, 4595-4601
• 5. EWOD-driven droplet microfluidic device integrated with optoelectronic tweezers as an automated platform for cellular isolation and analysis?
  Gaurav J. Shah,Eric P.-Y. Chiou,Ming C. Wu,Chang-Jin “CJ” Kim Lab Chip, 2009,9, 1732-1739

• 109216-60-6(Methyl 1-methyl-1H-indazole-3-carboxylate)
• 78155-74-5(Methyl 5-bromo-1H-indazole-3-carboxylate)
• 1021859-29-9(6-Bromo-1-methyl-1H-indazole-3-carboxylic acid)
• 1566649-43-1(Methyl 5-amino-1-methyl-1H-indazole-3-carboxylate)
• 885272-94-6(Ethyl 6-bromo-1H-indazole-3-carboxylate)
• 220488-05-1(Ethyl 1-methyl-1H-indazole-3-carboxylate)
• 1363380-96-4(5-Bromo-1-methyl-1H-indazole-3-carboxylic acid)
• 885278-42-2(Methyl 6-bromo-1H-indazole-3-carboxylate)
• 1190322-47-4(Methyl 4-bromo-1H-indazole-3-carboxylate)
• 1363173-34-5(1-Methyl-1H-indazole-3-carboxylic Acid Anhydride)