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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1372984Generated: October 31, 2026

1-Methylpiperazine → HCID 17974617, compound

https://huagongshe.com/reaction/1372984

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
ReactantHCID 21936045HCID 21936045—
SolventChloroformHCID 6212—
ProductHCID 17974617HCID 1797461775%

Reaction Steps

A solution of 7-(2,3-epoxypropoxy)-6-methoxy-3-(pivaloyloxymethyl)-3,4-dihydroquinazolin-4-one (5 g, 13.8 mmol) and N-methylpiperazine (1.7 ml) in chloroform (70 ml) was refluxed for 21 hours. After cooling the mixture was poured onto a column of silica and eluted with methanol/methylene chloride/ethylacetate (5/45/50) followed by (8/42/50) followed by methanol (saturated with ammonia)/ methylene chloride/methanol (5/45/50) followed by (8/42/50). The fractions containing the expected product were combined and the volatiles were removed under vacuum. The solid was triturated with ether, filtered, washed with ether and dried under vacuum to give 7-[2-hydroxy-3-(4-methylpiperazin-1-yl)propoxy]-6-methoxy-3-(pivaloyloxymethyl)-3,4-dihydroquinazolin-4-one (4.8 g, 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07160889B2
Source datasetuspto-grants-2007_01
ORD IDord-1dc07a30337d48a18359218900135333
Source noteuspto-grants-2007_01