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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2099377Generated: November 1, 2026

Chloroacetyl chloride → HCID 57794564, compound

https://huagongshe.com/reaction/2099377

Reaction equation

Participants

RoleNameHCIDCharge
ReactantChloroacetyl chlorideHCID 6577—
Reactant1-MethylpiperazineHCID 53167—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 68908613HCID 68908613—
SolventDichloromethaneHCID 6344—
ProductHCID 57794564HCID 57794564—

Reaction Steps

Chloroacetyl chloride (47 μl) was added to a solution of N-(3-chloro-2-fluorophenyl)-6-methoxy-7-[(3S)-piperidin-3-yloxy]quinazolin-4-amine dihydrochloride (250 mg) and diisopropylethylamine (373 μl) in methylene chloride (10 ml) and the mixture was stirred at ambient temperature for 1 hour. 1-Methylpiperazine (228 mg) was added, and the solution stirred for 1 hour before being washed with aqueous sodium hydroxide (2M, 10 ml) and water (10 ml). The organics were then purified by flash column chromatography eluting with methylene chloride/7N ammonia solution in methanol (97/3) to give a foam. This was re-precipitated by stirring in diethyl ether (20 ml) to give the title product as a white solid (0.135 g); 1H NMR Spectrum: (DMSO d6) 1.42-1.67 (m, 1H), 1.70-1.95 (m, 2H), 1.98-2.48 (m, 9H), 2.18 (s, 3H), 2.82-3.05 (m, 1H), 3.20-4.02 (m, 8H), 4.68 (m, 1H,), 7.30 (m, 1H), 7.34 (s, 1H), 7.44-7.60 (m, 2H), 7.82 (m, 1H), 8.38 (s, 1H), 9.64 (m, 1H); Mass Spectrum: (M+H)+ 543; melting point 120 to 121° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07569577B2
Source datasetuspto-grants-2009_08
ORD IDord-e474d81da0474e5aa2f65c8294895fd4
Source noteuspto-grants-2009_08