HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenesulfonyl chloride → 1h-Indole-2-carboxylic acid,3-phenyl-1-[[4-[(phenylsulfonyl)amino]phenyl]methyl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenesulfonyl chloride | HCID 7369 | — |
| Reactant | 1-(4-Amino-benzyl)-3-phenyl-1H-indole indolecarboxylic acid ethyl ester | HCID 69435471 | — |
| Product | 1h-Indole-2-carboxylic acid,3-phenyl-1-[[4-[(phenylsulfonyl)amino]phenyl]methyl]- | HCID 11317657 | — |
Reaction Steps
The title compound was prepared from 1-(4-amino-benzyl)-3-phenyl-1H-indole indolecarboxylic acid ethyl ester and benzenesulfonyl chloride followed the procedure of Example 3 Step 2 as an off-white solid: 1H NMR (DMSO-d6) δ 5.72 (s, 2H), 6.95-7.00 (m, 4H), 7.09-7.13 (m, 1H), 7.27-7.31 (m, 1H), 7.33-7.37 (m, 1H), 7.42-7.45 (m, 5H), 7.49-7.55 (m, 3H), 7.57-7.61 (m, 1H), 7.72 (dd, J=7.1, 1.4 Hz, 2H), 10.26 (br s, 1H), 12.83 (br s, 1H); MS (ESI) m/z 481 ([M−H]−); HRMS calcd for C28H21N2O4S: 481.1224; found (ESI−): 481.1228.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07268159B2 |
| Source dataset | uspto-grants-2007_09 |
| ORD ID | ord-f53bfaf9908840318d21eae85435b61b |
| Source note | uspto-grants-2007_09 |