HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 11352457, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 69231659 | HCID 69231659 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11352457 | HCID 11352457 | — |
Reaction Steps
The title compound was prepared from ethyl 5-amino-1-(1,1′-biphenyl-4-ylmethyl)-3-phenyl-1H-indole-2-carboxylate and methanesulfonyl chloride followed the procedure of Example 1 Step 3 as a white solid: 1H NMR (DMSO-d6) δ 2.86 (s, 3H, 5.87 (s, 2H), 7.22 (d, J=8.4 Hz, 2H, 7.25 (dd, J=9.0, 2.1 Hz, 1H, 7.30-7.40 (m, 3H, 7.40-7.50 (m, 6H), 7.58-7.63 (m, 4H, 7.66 (d, J=9.0 Hz, 1H, 9.40 (s, 1H, 12.52 (br s, 1H; MS (ESI) m/z 495 [M-H]−; HRMS calcd for C29H25N2O4S: 497.1533; found (ESI+): 497.1524; Anal. calcd for C29H24N2O4S.0.5H2O.0.5 ACN: C, 68.49; H, 5.05; N, 6.66. Found: C, 68.05; H, 5.04; N, 7.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442805B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-c5fb9c013a5c441f9c32b9e2275eabae |
| Source note | uspto-grants-2008_10 |