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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1416472Generated: November 2, 2026

Triethylamine → HCID 21309551, compound

https://huagongshe.com/reaction/1416472

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantBenzyl chloroformateHCID 10387—
ReactantHCID 21309555HCID 21309555—
SolventDichloromethaneHCID 6344—
ProductHCID 21309551HCID 21309551—

Reaction Steps

To a solution of 4-[(1R,4S)-[4-[(RS)-(tetrahydropyran-2-yl)oxy]cyclopent-2-en-1-yl]oxy]-2-(1-piperazinyl)quinazoline (11.07 g) in dry methylene chloride (110 ml) is added triethylamine (7.75 ml) with stirring under ice-cooling, and thereto is further added dropwise a solution of benzyl chlorocarbonate (4.40 ml) in dry methylene chloride (20 ml). The mixture is stirred under ice-cooling for one hour. The reaction mixture is washed with water, and dried over anhydrous magnesium sulfate. The solution is evaporated to dryness under reduced pressure, and the residue is purified by medium pressure liquid column chromatography (eluent, chloroform) to give 2-[4-(benzyloxycarbonyl)piperazin-1-yl]-4-[(1R,4S)-[4-[(RS)-(tetrahydropyran-2-yl)oxy]cyclopent-2-en-1-yl]oxy]quinazoline (12.57 g) as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05912247
Source datasetuspto-grants-1999_06
ORD IDord-efe6dca094cb4ae1ace3de94588021cc
Source noteuspto-grants-1999_06