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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841924Generated: November 2, 2026

Phosgene → 4-(4-Acryloylamino-benzenesulfonyl)-piperazine-1-carboxylic acid 2-chloro-benzyl ester

https://huagongshe.com/reaction/1841924

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
Reactant2-Chlorobenzyl alcoholHCID 28810—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamideHCID 56953730—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
Product4-(4-Acryloylamino-benzenesulfonyl)-piperazine-1-carboxylic acid 2-chloro-benzyl esterHCID 5293964412%

Reaction Steps

Phosgene (0.5 ml, 20% solution in toluene) was added in one portion to a stirred solution of 2-chlorobenzyl alcohol (0.1 g, 0.7 mmol) in THF (2 ml) and the resulting mixture was stirred at room temperature under a nitrogen atmosphere for 3 hours. After this time the reaction mixture was concentrated under vacuum and the resulting residue was diluted with DMF (2 ml) and added drop wise to a stirred solution of N-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamide (0.16 g, 0.54 mmol) and diisopropylethylamine (0.19 ml, 1.1 mmol) in DMF (4 ml). The resulting mixture was stirred at room temperature under a nitrogen atmosphere for 18 hours. After this time the reaction mixture was concentrated under vacuum and the residue was purified by Prep HPLC to give the title compound (0.029 g, 12% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946197B2
Source datasetuspto-grants-2015_02
ORD IDord-852b23af1f314c938a12cbf4ce4c30bc
Source noteuspto-grants-2015_02