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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosgene | HCID 6371 | — |
| Reactant | 2-Chlorobenzyl alcohol | HCID 28810 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-[4-(piperazine-1-sulfonyl)-phenyl]-acrylamide | HCID 56953730 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-Acryloylamino-benzenesulfonyl)-piperazine-1-carboxylic acid 2-chloro-benzyl ester | HCID 52939644 | 12% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08946197B2 |
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| Source dataset | uspto-grants-2015_02 |
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| ORD ID | ord-852b23af1f314c938a12cbf4ce4c30bc |
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| Source note | uspto-grants-2015_02 |
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