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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1063126Generated: November 1, 2026

Phosgene → HCID 69131963, compound

https://huagongshe.com/reaction/1063126

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantN,N-DiisopropylanilineHCID 61329—
Reactanttert-Butyl carbazateHCID 70091—
ReactantDiisopropylethylamineHCID 81531—
ReactantBenzyl piperazine-1-carboxylateHCID 643495—
SolventDichloromethaneHCID 6344—
ProductHCID 69131963HCID 69131963—

Reaction Steps

To a phosgene solution (20% solution in toluene) at 0° C. was added piperazine-1-carboxylic acid benzyl ester (0.385 mL, 1.996 mmol) and diisopropylphenyl amine (0.383 mL, 4.397 mmol) in 5 mL of CH2Cl2 dropwise. The resulting pale yellow mixture was stirred 2 h warming to room temperature under Ar. The phosgene solution was removed by vacuum distillation. 20 mL of anhydrous CH2Cl2 was added. The reaction vessel was cooled to 0° C. and hydrazinecarboxylic acid tert-butyl ester and diisopropylethyl amine (0.383 mL, 4.397 mmol) was added in one portion. The reaction was warmed to room temperature and stirred for 1 h. The reaction was quenched with 10 mL of saturated NaHCO3, diluted with 30 mL of EtOAc, then washed with 2×30 mL of saturated NH4Cl solution and 30 mL of brine. The organic phase was dried over MgSO4, filtered and concentrated to provide 720 mg of 4-(N-tert-butoxycarbonyl-hydrazinocarbonyl)-piperazine-1-carboxylic acid benzyl ester as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06964956B2
Source datasetuspto-grants-2005_11
ORD IDord-dd8bf535f7bd4c028810579529d7488e
Source noteuspto-grants-2005_11