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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094974Generated: November 2, 2026

Pyridine → HCID 86608143, compound

https://huagongshe.com/reaction/1094974

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantVeratroyl chlorideHCID 77070—
ReactantEthyl 2-amino-4-methylthiophene-3-carboxylateHCID 521132—
ProductHCID 86608143HCID 86608143—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl 2-amino-4-methylthiophene-3-carboxylate (compound A) (3.0 g) was dissolved in anhydrous methylene chloride (40.0 ml). Subsequently, pyridine (1.5 ml) and 3-(chloromethyl)benzoyl chloride (compound B) (2.8 ml) were added to the solution, and the mixture was stirred at 0° C. for one hr. After the completion of the reaction, distilled water was added, and the mixture was subjected to separatory extraction with chloroform. The organic layer was washed with saturated brine, was dried over sodium sulfate, and was then concentrated to give 2-(3-chloromethyl-benzoylamino-4-methyl-thiophene-3-carboxylic acid ethyl ester as a useful intermediate (3.80 g, yield 70%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-ab7f2862b9af48de90d03f1fab5b41a2
Source noteuspto-grants-2012_03