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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1695740Generated: October 31, 2026

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

https://huagongshe.com/reaction/1695740

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 DCM (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 numberUS08163743B2
Source datasetuspto-grants-2012_04
ORD IDord-a1b85bcd996b4b8b90c3117eef7f7687
Source noteuspto-grants-2012_04