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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2246782Generated: November 1, 2026

Ammonia → 1-(6-Chloro-3-pyridinyl)cyclopropanecarboxamide

https://huagongshe.com/reaction/2246782

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantTriethylamineHCID 8471—
ReactantIsobutyl chloroformateHCID 62365—
Reactant1-(6-Chloropyridin-3-yl)cyclopropane-1-carboxylic acidHCID 59216308—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
Product1-(6-Chloro-3-pyridinyl)cyclopropanecarboxamideHCID 71743267—

Reaction Conditions

Temperature0 °C

Reaction Steps

To a 0° C. solution of 1-(6-chloropyridin-3-yl)cyclopropanecarboxylic from Step 4 (1.0 g) in chloroform (50 mL) were slowly added isobutyl chloroformate (800 μL) and triethylamine (920 μL). The reaction mixture was stirred at 0° C. for 2 hours. Then it was saturated with ammonia gas and stirred at 0° C. for 10 minutes. The reaction mixture was allowed to stand at room temperature for 1 hour then poured into water (80 mL) and partitioned. The aqueous layer was extracted with dichloromethane (2×80 mL). The combined extracts were washed with brine, dried with magnesium sulfate and the solvent removed in vacuo. The residue was purified by swish using diethyl ether and hexanes to yield the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07687524B2
Source datasetuspto-grants-2010_03
ORD IDord-d2390e9d5fcb4aec8f8717a51dfac4ca
Source noteuspto-grants-2010_03