HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Phenoxybenzoyl chloride → N-[1-Cyano-2-(5,7-dichloro-2H-indazol-2-yl)-1-methylethyl]-4-phenoxybenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Phenoxybenzoyl chloride | HCID 74193 | — |
| Reactant | 2-amino-2-methyl-3-(5,7-dichloro-2H-indazol-2-yl)propionitrile | HCID 66620022 | — |
| Product | N-[1-Cyano-2-(5,7-dichloro-2H-indazol-2-yl)-1-methylethyl]-4-phenoxybenzamide | HCID 66620412 | — |
Reaction Steps
Using a procedure similar to that described in Example 1, except using 2-amino-2-methyl-3-(5,7-dichloro-2H-indazol-2-yl)propionitrile (60 mg, described in Example 109) and 4-phenoxybenzoyl chloride, the title compound was isolated as a white solid (90 mg, 87%). MS (ES): M/Z [M+H]=465. 1H NMR: (400 MHz, DMSO-d6): 1.71 (s, 3H), 5.12 (d, 1H), 5.21 (d, 1H), 7.04-7.13 (m, 4H), 7.23 (t, J=7.4 Hz, 1H), 7.41-7.51 (m, 3H), 7.85-7.92 (m, 3H), 8.52 (s, 1H) and 8.80 (s, 1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08461176B2 |
| Source dataset | uspto-grants-2013_06 |
| ORD ID | ord-9cd0044a16cc42bcaaa9f7ab9a0b8a4b |
| Source note | uspto-grants-2013_06 |