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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1497944Generated: October 30, 2026

Methyl chloroformate → HCID 71280654, compound

https://huagongshe.com/reaction/1497944

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl chloroformateHCID 6586—
ReactantHCID 71280501HCID 71280501—
SolventPyridineHCID 1049—
ProductHCID 71280654HCID 71280654—

Reaction Steps

To a stirring solution of N-(5-(5-(1-amino-3,3-difluorocyclobutyl)-1,2,4-oxadiazol-3-yl)-2-methylphenyl)imidazo[1,2-a]pyridine-3-carboxamide hydrochloride (166) in anhydrous pyridine (1 mL) at 0° C. was added drop-wise methyl chloroformate (19 uL, 0.26 mmol). The reaction was stirred to room temperature for 20 minutes. The crude was concentrated and purified by preparative HPLC to yield methyl (3,3-difluoro-1-(3-(3-(imidazo[1,2-a]pyridine-3-carboxamido)-4-methylphenyl)-1,2,4-oxadiazol-5-yl)cyclobutyl)carbamate (F174). MS m/z 483.1 (M+1)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09199981B2
Source datasetuspto-grants-2015_12
ORD IDord-b4652fb7c8c74a5db28b114a478bfe9f
Source noteuspto-grants-2015_12