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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071278Generated: November 3, 2026

Pyridine → HCID 22397891, compound

https://huagongshe.com/reaction/1071278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantDichloromethaneHCID 6344—
Reactant2,6-Dichlorobenzoyl chlorideHCID 78392—
ReactantHCID 20610283HCID 20610283—
SolventEthyl AcetateHCID 8857—
ProductHCID 22397891HCID 2239789180.3%

Reaction Steps

A dichloromethane (1 mL) solution 2-allyloxycarbonylamino-3-(3-{1-[(4-amino-phenyl)-acetyl]-pyrrolidin-2-yl}-isoxazol-5-yl)-propionic acid ethyl ester (80 mg, 0.170 mmol) was cooled to 0° C. and 2,6-dichlorobenzoylchloride (39 mg, 0.187 mmol) was added. The mixture was stirred for 15 minutes then pyridine (28 μL, 0.34 mmol) was added. The reaction was slowly warmed to room temperature and stirred overnight. The reaction was diluted with ethyl acetate and washed with water, 1M sodium hydroxide and brine. The organic portion was dried over magnesium sulfate and concentrated to give the title compound (84 mg, 78%). MS (Cl) m/z 635.3 (M+1), 632.5 (M−1) C. 2-Allyloxycarbonylamino-3-(3-{1-[(4-amino-phenyl)-acetyl]-pyrrolidin-2-yl}-isoxazol-5-yl)propionic acid ethyl ester

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903128B2
Source datasetuspto-grants-2005_06
ORD IDord-35cd1ddd26ff4ff0ab21c3c51a31114e
Source noteuspto-grants-2005_06