HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Methoxy-4-methylbenzene-1-sulfonyl chloride → 2-Methoxy-4-methyl-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Methoxy-4-methylbenzene-1-sulfonyl chloride | HCID 11345048 | — |
| Reactant | N-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamide | HCID 22272479 | — |
| Product | 2-Methoxy-4-methyl-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide | HCID 10279475 | — |
Reaction Steps
2-Methoxy-4-methyl-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and 2-methoxy-4-methylbenzenesulfonylchloride (53 mg, 0.239 mmol) according to general method 3 to give 80 mg of a purple solid. MS (posES-FIA) m/z=Found: 517.2; Calcd 517.15; 1H NMR δ 7.67-7.37 (m, 6H), 7.10-7.04 (m, 2H), 6.97-6.74 (m, 2H), 6.30 (d, 1H), 4.06 (s, 3H), 3.26-3.09 (m, 8H), 2.37 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07718650B2 |
| Source dataset | uspto-grants-2010_05 |
| ORD ID | ord-e6d536ac72444aaea6d9e022deb1c276 |
| Source note | uspto-grants-2010_05 |