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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1052170Generated: October 31, 2026

Triethylamine → HCID 71147160, compound

https://huagongshe.com/reaction/1052170

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantPyrrolidineHCID 31268—
ReactantChloro(phenyl)acetyl chlorideHCID 102902—
Reactant3-Amino-5-bromothiophene-2-carboxamideHCID 21975862—
SolventTetrahydrofuranHCID 8028—
ProductHCID 71147160HCID 71147160—

Reaction Steps

To a mixture of 3-amino-5-bromothiophene-2-carboxamide (221 mg) produced in Example 1, step D, triethylamine (0.153 mL) and tetrahydrofuran (5.0 mL) was added chloro(phenyl)acetylchloride (0.174 mL) with stirring at room temperature. The reaction mixture was stirred for 10 min, and pyrrolidine (0.42 mL) was added. The reaction mixture was stirred with heating at 70° C. for 1 hr, and the reaction system was concentrated under reduced pressure. To the residue was added 2M aqueous sodium hydroxide solution (1.5 mL), and the mixture was stirred with heating at 120° C. for 2 hr. The mixture was extracted with ethyl acetate and dried over anhydrous sodium sulfate. Insoluble material was removed by filtration, and the filtrate was concentrated under reduced pressure. The residue was purified by basic silica gel column chromatography (ethyl acetate/hexane). The obtained yellow solid was washed with ethyl acetate (2 mL) to give the title compound (330 mg) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09388195B2
Source datasetuspto-grants-2016_07
ORD IDord-1293564f8f51472cafe425b91de0c339
Source noteuspto-grants-2016_07