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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1015616Generated: November 1, 2026

4-Chlorobenzoyl chloride → HCID 20775759, compound

https://huagongshe.com/reaction/1015616

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Chlorobenzoyl chlorideHCID 8501—
ReactantMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
SolventPyridineHCID 1049—
ProductHCID 20775759HCID 2077575991.1%

Reaction Steps

To mixture of methyl-3-amino-5-phenylthiophene-2-carboxylate (100 mg, 0.428 mmol) in anhydrous pyridine (4.3 ml) was added p-chlorobenzoyl chloride (71 μl, 0.556 mmol). The mixture was stirred for 3 hours at room temperature and concentrated. Purification chromatography (silica gel, hexane to hexane:ethyl acetate; 95:5) gave 145 mg (91% yield) of 3-(4-Chloro-benzoylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester. 1H NMR (CDC3, 400 MHz) 8.54 (s, 1H), 7.99-7.96 (m, 2H), 7.73-7.71 (m, 2H); 7.52-7.50 (m, 2H), 7.46-7.39 (m, 3H), 3.95 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07985769B2
Source datasetuspto-grants-2011_07
ORD IDord-d090cd4b49b94fa597d68251a5bacae7
Source noteuspto-grants-2011_07