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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 880519Generated: November 1, 2026

Oxalyl chloride → HCID 86654678, compound

https://huagongshe.com/reaction/880519

Reaction equation

Participants

RoleNameHCIDCharge
ReactantOxalyl chlorideHCID 65578—
ReactantHCID 66914904HCID 66914904—
SolventChloroformHCID 6212—
ProductHCID 86654678HCID 86654678—

Reaction Steps

Oxalyl chloride (0.19 g, 1.53 mmol) was added to a solution of 1-(2-methoxy-ethyl)-2-methyl-4-phenyl-1H-pyrrole (0.30 g, 1.39 mmol) in chloroform (5 mL) at 0° C. and slowly warmed the ambient temperature to RT over 30 min. Completion of reaction and removal of excess oxalyl chloride in vacuo afforded the intermediate acid chloride, [1-(2-methoxy-ethyl)-5-methyl-3-phenyl-1H-pyrrol-2-yl]-oxo-acetyl chloride which was taken in chloroform (5 mL). This was then added to a solution of 3-fluoro-4-morpholin-4-yl-phenylamine (0.19 g, 0.97 mmol) in chloroform (5 mL) with triethyl amine (0.28 g, 2.78 mmol). The reaction was stirred for 30 min at ambient temperature and then diluted with water and extracted into chloroform. Combined organic extracts were washed with saturated bicarbonate solution, dried over anhydrous sodium sulfate and stirred over neutral alumina for 10 min. The mixture was filtered and concentrated in vacuo to afford N-(3-fluoro-4-morpholin-4-yl-phenyl)-2-[1-(2-methoxy-ethyl)-5-methyl-3-phenyl-1H-pyrrol-2-yl]-2-oxo-acetamide (0.26 g, 40%) as pale yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08993574B2
Source datasetuspto-grants-2015_03
ORD IDord-731ca4aefc0d4e5db5e3dd245ed2c3de
Source noteuspto-grants-2015_03