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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 500127Generated: October 31, 2026

Chloroacetaldehyde → 2-fluoro-4-imidazo[1,2-a]pyrimidin-6-yl-N-methylbenzamide

https://huagongshe.com/reaction/500127

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetaldehydeHCID 33—
Reactant4-(2-aminopyrimidin-5-yl)-2-fluoro-N-methylbenzamideHCID 67224548—
SolventIsopropanolHCID 3776—
Product2-fluoro-4-imidazo[1,2-a]pyrimidin-6-yl-N-methylbenzamideHCID 6722485188.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

A mixture of 4-(2-aminopyrimidin-5-yl)-2-fluoro-N-methylbenzamide (123 mg, 0.5 mmol) and chloroacetaldehyde (0.318 mL, 2.5 mmol) in isopropyl alcohol (4 mL) was stirred at 90° C. for 4 h. The solvent was removed under vacuum and the residue was triturated with ethyl acetate and hexanes. The solid formed was collected and dried under reduced pressure to give the desired product (120 mg, 88.8%). LCMS: (M+H)=271.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07767675B2
Source datasetuspto-grants-2010_08
ORD IDord-b4befdcaa61a4a2a8f5d493dfd20df7c
Source noteuspto-grants-2010_08