HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Butoxybenzenesulfonyl Chloride → HCID 10187338, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Butoxybenzenesulfonyl Chloride | HCID 517990 | — |
| Reactant | N-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamide | HCID 22272479 | — |
| Product | HCID 10187338 | HCID 10187338 | — |
Reaction Steps
4-Butoxy-N-[2-[(phenylsulfonyl)amino]-4-(1-piperazinyl)phenyl]benzenesulfonamide was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and 4-n-butoxybenzenesulfonylchloride (59 mg, 0.239 mmol) according to general method 3 to give 70 mg of a purple solid. MS (posES-FIA) m/z=Found: 545.2. Calcd 545.18. 1H-NMR δ 7.73-7.45 (m, 7H), 6.95-6.91 (m, 2H), 6.72-6.70 (m, 1H), 4.00 (t, 2H), 3.29-3.24 (m, 8H), 1.79-1.70 (m, 2H), 1.55-1.43 (m, 2H), 0.97 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06969710B2 |
| Source dataset | uspto-grants-2005_11 |
| ORD ID | ord-0b87eb9552df4972b5d4d27adc16e74e |
| Source note | uspto-grants-2005_11 |