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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2224091Generated: November 2, 2026

Pyridine → HCID 3573095, compound

https://huagongshe.com/reaction/2224091

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantButyryl chlorideHCID 8855—
ReactantMethyl 3-amino-2-thiophenecarboxylateHCID 89652—
SolventDichloromethaneHCID 6344—
ProductHCID 3573095HCID 3573095—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a flame dried flask equipped with stir bar was added methyl 3-aminothiophene-2-carboxylate (2.06 g, 13.1 mmol) and anhydrous methylene chloride (10.0 mL). The resulting solution was cooled to 0° C., and treated successively with pyridine (1.11 mL, 13.7 mmol) and butyryl chloride (1.44 mL, 13.7 mmol) while stirring under N2. The ice bath was removed, and the reaction warmed to 25° C. and stirred 3 h. The reaction was then poured into 1N HCl and extracted with methylene chloride. The combined organics were dried over magnesium sulfate, filtered and concentrated to provide methyl 3-(butyrylamino)thiophene-2-carboxylate (1-2). MS 228 found, 227.3 required.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07378411B2
Source datasetuspto-grants-2008_05
ORD IDord-e389dc6669904a4e9b8feb59ea52fb0a
Source noteuspto-grants-2008_05