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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1094978Generated: November 1, 2026

Pyridine → HCID 66638494, compound

https://huagongshe.com/reaction/1094978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
ReactantVeratroyl chlorideHCID 77070—
ReactantHCID 53438117HCID 53438117—
ProductHCID 66638494HCID 66638494—

Reaction Conditions

Temperature0 °C

Reaction Steps

Ethyl-2-aminocyclopenta(B)thiophene-3-carboxylate (compound A) (1.0 g) was dissolved in anhydrous methylene chloride (20.0 ml). Subsequently, pyridine (760 μl) and 3-(chloromethyl)benzoyl chloride (compound B) (880 μl) were added to the solution at 0° C., and the mixture was stirred at 0° C. for one hr. After the completion of the reaction, distilled water was added thereto, 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)-5,6-dihydro-4H-cyclopenta[b]thiophene-3-carboxylic acid ethyl ester as a useful intermediate (800 mg, crude yield 100%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08134015B2
Source datasetuspto-grants-2012_03
ORD IDord-aa6646a089d24655a682bf18443e7b3a
Source noteuspto-grants-2012_03