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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363075Generated: October 30, 2026

5-Chlorothiophene-2-carbonyl Chloride → HCID 57572393, compound

https://huagongshe.com/reaction/1363075

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chlorothiophene-2-carbonyl ChlorideHCID 589223—
ReactantHCID 57572395HCID 57572395—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventPyridineHCID 1049—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 57572393HCID 57572393—

Reaction Steps

300 mg of tert-butyl 5-(3-amino-1H-indazol-5-yl)furan-2-carboxylate, 199 mg of 5-chlorothiophene-2-carbonyl chloride and 8 mg of 4-(dimethylamino)pyridine are stirred at 90° C. for 24 hours in 2 ml of pyridine and 100 μl of dioxane. The reaction mixture is evaporated, and the residue is purified by column chromatography. Yield: 260 mg (58%) of tert-butyl 5-{3-[(5-chlorothiophene-2-carbonyl)amino]-1H-indazol-5-yl}furan-2-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07884126B2
Source datasetuspto-grants-2011_02
ORD IDord-c8e8ff20376f43459c256e76affaf733
Source noteuspto-grants-2011_02