HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetamide, N-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]- → 4-(4-Methylpiperazine-1-sulfonyl)aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetamide, N-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]- | HCID 764494 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-(4-Methylpiperazine-1-sulfonyl)aniline | HCID 567261 | 53% |
Reaction Steps
N-[4-(4-methylpiperazine-1-sulfonyl)phenyl]acetamide (2 g, 6.7 mmol) was dissolved in 3 N HCl (50 mL) and 1,4-dioxane (12 mL). The reaction mixture was refluxed for 1 h, evaporated under vacuum, and the rsulting mixture made basic with 30% NH4OH. The desired product was extracted with CH2Cl2, dried (Na2SO4), filtered, and evaporated under reduced pressure to obtain 4-(4-methylpiperazin-1-sulfonyl)aniline as a white solid. MP: 210° C.; Yield 53%; 1H NMR (DMSO d6): δ 2.22 (s, 3H), 2.50 (m, 4H), 2.82 (m, 4H), 6.10 (bs, 2H), 6.62-6.67 (d, 2H, J=10 Hz), 7.32-7.36 (d, 2H, J=8 Hz).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921825B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-e4862aa52d994269aa1a4a38d2d081a0 |
| Source note | uspto-grants-2005_07 |