ChemicalBook--->CAS DataBase List--->1346702-54-2

1346702-54-2

1346702-54-2 Structure

1346702-54-2 Structure
IdentificationBack Directory
[Name]

6-BROMO-1-ISOPROPYL-1H-INDAZOLE-4-CARBOXYLIC ACID
[CAS]

1346702-54-2
[Synonyms]

6-bromo-1-propan-2-ylindazole-4-carboxylic acid
6-BROMO-1-ISOPROPYL-1H-INDAZOLE-4-CARBOXYLIC ACID
6-bromo-1-(propan-2-yl)-1H-indazole-4-carboxylic acid
1H-Indazole-4-carboxylic acid, 6-bromo-1-(1-methylethyl)-
[Molecular Formula]

C11H11BrN2O2
[MDL Number]

MFCD26407123
[MOL File]

1346702-54-2.mol
[Molecular Weight]

283.12
Chemical PropertiesBack Directory
[storage temp. ]

Sealed in dry,Room Temperature
[Appearance]

White to off-white Solid
Spectrum DetailBack Directory
[Spectrum Detail]

6-BROMO-1-ISOPROPYL-1H-INDAZOLE-4-CARBOXYLIC ACID(1346702-54-2)1HNMR
Hazard InformationBack Directory
[Synthesis]

Methyl 6-broMo-l-(l- Methylethyl)-lH-indazole-4-carboxylate

1346702-52-0

6-BROMO-1-ISOPROPYL-1H-INDAZOLE-4-CARBOXYLIC ACID

1346702-54-2

b) Methyl 6-bromo-1-isopropyl-1H-indazole-4-carboxylate (0.58 g, 1.952 mmol) was dissolved in a solvent mixture of methanol (12 mL) and tetrahydrofuran (3 mL). A 3N NaOH solution (3.25 mL, 9.76 mmol) was added slowly via syringe and the reaction mixture was stirred at room temperature for 3 hours. Upon completion of the reaction, the volatile solvent was removed under vacuum and the residue was diluted with water and the pH was adjusted to 4-5 by slow dropwise addition of 1 N HCl. The aqueous phase was extracted with a 20% THF/EtOAc solvent mixture (3 times). The organic phases were combined, washed with saturated brine, dried over anhydrous MgSO4, filtered and concentrated to afford 6-bromo-1-isopropyl-1H-indazole-4-carboxylic acid (0.52 g, 94% yield). The product was characterized by 1H NMR (400 MHz, DMSO-d6) and LC-MS (ES): 1H NMR δ 13.54 (s, 1H), 8.36-8.43 (m, 2H), 7.82 (d, J = 1.52 Hz, 1H), 5.11 (quin, J = 6.57 Hz, 1H), 1.48 (s, 3H), 1.47 ( s, 3H); LC-MS (ES) [M + H]+ 283.4/285.2.

[References]

[1] Patent: WO2011/140325, 2011, A1. Location in patent: Page/Page column 41
[2] ACS Medicinal Chemistry Letters, 2012, vol. 3, # 12, p. 1091 - 1096
[3] Patent: WO2012/118812, 2012, A2. Location in patent: Page/Page column 320-321
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