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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1841926Generated: November 2, 2026

Phosgene → N-{4-[4-(Piperidine-1-carbonyl)-piperazine-1-sulfonyl]-phenyl}-acrylamide

https://huagongshe.com/reaction/1841926

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosgeneHCID 6371—
ReactantPiperidineHCID 8082—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamideHCID 56953730—
SolventDimethylformamideHCID 6228—
SolventTetrahydrofuranHCID 8028—
ProductN-{4-[4-(Piperidine-1-carbonyl)-piperazine-1-sulfonyl]-phenyl}-acrylamideHCID 5293804614%

Reaction Steps

Phosgene (0.5 ml, 20% solution in toluene) was added in one portion to a stirred solution of piperidine (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 (0.032 g, 14% yield) as a white powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08946197B2
Source datasetuspto-grants-2015_02
ORD IDord-0d5a1e71be314f479af632b7ae1553dc
Source noteuspto-grants-2015_02