HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanobenzoyl chloride → 4-cyano-N-(8H-indeno[1,2-d]thiazol-2-yl)benzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| Reactant | HCID 49796119 | HCID 49796119 | — |
| Product | 4-cyano-N-(8H-indeno[1,2-d]thiazol-2-yl)benzamide | HCID 3298604 | 25.6% |
Reaction Steps
Acylation of 8H-Indeno[1,2-d]thiazol-2-ylamine hydroiodide 1a (Prepared in Example 1, Step 1, 100 mg; 0.32 mmol) with 4-cyanobenzoyl chloride (164 mg; 0.96 mmol) in a manner similar to that described in Example 1, Step 3 provided 26 mg of 4-Cyano-N-(8H-indeno[1,2-d]thiazol-2-yl)-benzamide 4. EI-HRMS m/e calcd for C18H14N2OS (M+) 306.0827, found 306.0827.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07407977B2 |
| Source dataset | uspto-grants-2008_08 |
| ORD ID | ord-3dc5a2c4778144b783a061da2e7ff5d8 |
| Source note | uspto-grants-2008_08 |