HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl vinyl ketone → 1-{4-[2-(3-Chloro-phenyl)-5-methyl-pyrrol-1-yl]-benzenesulfonyl}-piperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl vinyl ketone | HCID 6570 | — |
| Reactant | 3-Chlorobenzaldehyde | HCID 11477 | — |
| Reactant | 4-(Piperidine-1-sulfonyl)aniline | HCID 236648 | — |
| Product | 1-{4-[2-(3-Chloro-phenyl)-5-methyl-pyrrol-1-yl]-benzenesulfonyl}-piperidine | HCID 68484323 | — |
Reaction Steps
3-Chlorobenzaldehyde and but-3-en-2-one were treated according to the procedure outlined in General Procedure C followed by subjecting the resulting product to conditions outlined in General Procedure D along with p-piperidinylsulfonyl phenylamine to obtain the titled compound. 1H NMR (CDCl3) δ ppm 1.42-1.65 (6H), 2.18 (3H), 3.00 (4H), 6.18 (1H), 6.40 (1H), 6.85-7.90 (8H); MS (ESI) m/z 415 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741364B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-2d32fddd135b41969e460b8bf3491573 |
| Source note | uspto-grants-2010_06 |