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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1398578Generated: October 26, 2026

Dimethylformamide → 1-(2-Aminopyrimidin-4-yl)-6-bromoindazole-3-carboxamide

https://huagongshe.com/reaction/1398578

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantThionyl ChlorideHCID 24386—
Reactant1-(2-Aminopyrimidin-4-yl)-6-bromoindazole-3-carboxylic acidHCID 68181966—
SolventDichloromethaneHCID 6344—
Product1-(2-Aminopyrimidin-4-yl)-6-bromoindazole-3-carboxamideHCID 68181625—

Reaction Steps

To a solution of 1-(2-aminopyrimidin-4-yl)-6-bromoindazole-3-carboxylic acid (500 mg, 1.32 mmol) in DCM (5 mL), was added thionyl chloride (0.6 mL, 7.9 mmol) followed by DMF (0.02 mL). The mixture was stirred at RT for 1 hr. The mixture was concentrated in vacuo, DCM (2 mL) added and concentration in vacuo was repeated. To this residue was added THF (5 mL) and conc. aq NH3 (0.5 mL). The mixture stirred for 30 min, then diluted with water and the resultant solid was collected by suction filtration. The solid was thoroughly dried under high vacuum, to give the title compound (360 mg): 1H NMR (250 MHz, DMSO) delta 7.15 (1H, br. s.), 7.32 (1H, d, J=5.48 Hz), 7.60 (1H, dd, J=8.60, 1.60 Hz), 7.74 (1H, br. s.), 8.20 (1H, d, J=8.38 Hz), 8.38 (1H, d, J=5.48 Hz), 9.18 (1H, d, J=1.22 Hz); LC-MS: m/z=+332.90/334.70 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08901313B2
Source datasetuspto-grants-2014_12
ORD IDord-4991ad4935c94f43aa411df6a445dba3
Source noteuspto-grants-2014_12