HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dansyl chloride → 5-(Dimethylamino)-N-{4-(1-piperazinyl)-2-[(phenylsulfonyl)amino]phenyl}-1-naphthalenesulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dansyl chloride | HCID 11801 | — |
| Reactant | N-(2-amino-5-(4-boc-1-piperazinyl)-phenyl)-benzenesulfonamide | HCID 22272479 | — |
| Product | 5-(Dimethylamino)-N-{4-(1-piperazinyl)-2-[(phenylsulfonyl)amino]phenyl}-1-naphthalenesulfonamide | HCID 10120539 | — |
Reaction Steps
5-(Dimethylamino)-N-{4-(1-piperazinyl)-2-[(phenylsulfonyl)amino]phenyl}-1-naphthalenesulfonamide was synthesized from N-{2-amino-5-(4-t-butyloxycarbonyl-piperazinyl)-phenyl}benzenesulfonamide and dansylchloride (64 mg, 0.239 mmol) according to general method 3 to give 60 mg of a purple solid. MS (posES-FIA) m/z=Found: 566.3; Calcd: 566.18; 1H NMR δ 8.84 (d, 1H), 8.60 (d, 1H), 8.08 (d, 2H), 7.84–7.47 (m, 7H), 6.70 (d, 1H), 6.56–6.53 (m, 1H), 6.41–6.37 (m, 1H), 3.46 (s, 6H), 3.25–3.12 (m, 8H),
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07173035B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-c9522575ae8c40e7813c162e1e45579b |
| Source note | uspto-grants-2007_02 |