HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanesulfonyl chloride → HCID 11317958, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | HCID 69227813 | HCID 69227813 | — |
| Product | HCID 11317958 | HCID 11317958 | — |
Reaction Steps
The title compound was prepared from ethyl 5-amino-1-benzhydryl-3-phenyl-1H-indole-2-carboxylate and methanesulfonyl chloride followed the procedure of Example 1 Step 3 as an off-white solid: 1H NMR (DMSO-d6) δ 2.85 (s, 3H, 6.79 (d, J=9.0 Hz, 1H, 6.95 (dd, J=9.0, 2.0 Hz, 1H, 7.19 (d, J=7.4 Hz, 4H, 7.30-7.50 (m, 12H, 7.91 (s, 1H, 9.37 (s, 1H, 13.21 (br s, 1H; MS (ESI) m/z 495 [M-H]−; HRMS calcd for C29H25N2O4S: 497.1533; found (ESI+): 497.1522; Anal. calcd for C29H24N2O4S.0.7H2O: C, 68.41; H, 5.03; N, 5.50. Found: C, 68.32; H, 4.91; N, 5.70.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07442805B2 |
| Source dataset | uspto-grants-2008_10 |
| ORD ID | ord-561ad9d8698d40789df1dba30c66628d |
| Source note | uspto-grants-2008_10 |