Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244716Generated: October 30, 2026

Pyridine → N-(6-Bromo-1-methyl-1H-indazol-4-yl)-2-(chloromethyl)-4-thiazolecarboxamide

https://huagongshe.com/reaction/244716

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSodium BicarbonateHCID 516892—
Reactant4-(chloromethyl)-1,3-thiazole-2-carbonyl ChlorideHCID 10607914—
ReactantHCID 58255771HCID 58255771—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductN-(6-Bromo-1-methyl-1H-indazol-4-yl)-2-(chloromethyl)-4-thiazolecarboxamideHCID 58255850—

Reaction Conditions

Temperature0 °C

Reaction Steps

6-Bromo-1-methyl-1H-indazol-4-amine (1 g, 4.42 mmol) was dissolved in dichloromethane (DCM) (10 mL) and pyridine (0.429 mL, 5.31 mmol) added. The mixture was cooled to 0° C. in an ice-water bath and 4-(chloromethyl)-1,3-thiazole-2-carbonyl chloride (0.867 g, 4.42 mmol) in DCM (10 ml) was added portionwise over 5 mins. The mixture was stirred for 2 hours and allowed to warm to room temperature. Saturated sodium bicarbonate solution (15 ml) was added and the mixture stirred vigorously for 10 mins. The mixture was diluted with water (50 ml) and DCM (50 ml), but a precipitate was still present. This was collected by filtration, washed with DCM and air dried to afford the title compound as a yellow/brown solid (860 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08658635B2
Source datasetuspto-grants-2014_02
ORD IDord-6777d20b6c0948dfb31836ffe213e667
Source noteuspto-grants-2014_02