HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → Acetamide, N-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-Acetylsulfanilyl chloride | HCID 8481 | — |
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Acetamide, N-[4-[(4-methyl-1-piperazinyl)sulfonyl]phenyl]- | HCID 764494 | 41% |
Reaction Steps
A suspension of 4-acetylaminobenzene sulfonyl chloride (4.5 mmol) in anhydrous CH2Cl2 at room temperature is treated with 1-methyl piperazine (4.5 mmol) and triethylamine (4.5 mmol). The reaction mixture was stirred at room temperature for 1 hour, water was added, and the product extracted with additional CH2Cl2. The combined organic extracts were dried (Na2SO4), filtered, and evaporated under reduced pressure, affording the desired N-[4-(4-methylpiperazine-1-sulfonyl)phenyl]acetamide. Mp: 184° C.; Yield 41%; 1H NMR (DMSO d8): δ 2.09 (s, 3H), 2.15 (s, 3H), 2.40 (m, 4H), 2.85 (m, 4H), 7.63-7.68 (d,2H, J=10 Hz), 7.80-7.84 (d, 2H, J=8 Hz), 10.41 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06921825B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-303b5ac1a0624e2a82cadcbd8b626322 |
| Source note | uspto-grants-2005_07 |