HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 337225Generated: October 30, 2026
Acryloyl chloride → HCID 71618411, compound
https://huagongshe.com/reaction/337225
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acryloyl chloride | HCID 13140 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 71060145 | HCID 71060145 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 71618411 | HCID 71618411 | 4.2% |
Reaction Steps
Diisopropylethylamine (0.09 ml, 0.56 mmol) was added in one portion to a stirred solution of N-[4-(4-Amino-piperidine-1-sulfonyl)-2-chloro-phenyl]-3-phenyl-propionamide (0.05 g, 0.1 mmol) in THF (5 ml), followed by the drop wise addition of acryloyl chloride (0.01 ml, 0.12 mmol) and the mixture was stirred at room temperature under a nitrogen atmosphere for 3 hours. After this time the mixture was diluted with DCM (20 ml) and washed sequentially with HCl (1M solution, 10 ml), NaOH (1M solution, 10 ml) and brine (10 ml). The organic layer was separated, dried (MgSO4), filtered, concentrated and the resulting residue was purified by flash column chromatography (elution: 2% Methanol, 98% DCM) to give the title compound (0.002 g, 4% yield) as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08889716B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-ec2b5e8f899a4f6eb7e691153e4b6266 |
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| Source note | uspto-grants-2014_11 |
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