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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1953433Generated: November 1, 2026

Triethylamine → phenylmethyl 1-[N-[4-(methoxycarbonyl)piperazine-1-carbonyl]amino]cyclohexanecarboxylate

https://huagongshe.com/reaction/1953433

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantChloromethylcarbonateHCID 21717543—
Reactantphenylmethyl 1-[N-(piperazine-1-carbonyl)amino]cyclohexanecarboxylateHCID 23297891—
SolventDichloromethaneHCID 6344—
Productphenylmethyl 1-[N-[4-(methoxycarbonyl)piperazine-1-carbonyl]amino]cyclohexanecarboxylateHCID 2329795598.1%

Reaction Steps

Subsequently, 0.98 ml (2.83 mmol) of the phenylmethyl 1-[N-(piperazine-1-carbonyl)amino]cyclohexanecarboxylate and 0.39 ml (2.83 mmol) of triethylamine were dissolved in 20 ml of anhydrous methylenechloride and then 0.21 ml (2.83 mmol) of chloromethylcarbonate was added to the above prepared mixture and stirred for 12 hours at the room temperature. The reaction solution was successively washed with 1N hydrochloric acid, saturated sodium hydrogen-carbonate solution and saturated brine, and dried over anhydrous sodium sulfate and concentrated under reduced pressure, whereby 1.12 g of phenylmethyl 1-[N-[4-(methoxycarbonyl)piperazine-1-carbonyl]amino]cyclohexanecarboxylate was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06117870
Source datasetuspto-grants-2000_09
ORD IDord-fa4ad9c6123c4849a846ce89fe2ee76c
Source noteuspto-grants-2000_09