HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Cyanobenzoyl chloride → HCID 15407873, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyanobenzoyl chloride | HCID 80172 | — |
| Reactant | HCID 15407881 | HCID 15407881 | — |
| Product | HCID 15407873 | HCID 15407873 | — |
Reaction Steps
4-Cyano-N-methyl-N-(4-picolyl)benzamide The title compound was prepared using the same procedure as described in Example 2, step (b) except using 4-cyanobenzoyl chloride: 1H NMR (CDCl3): d 8.49 (dd, 2H); 7.86-7.04 (m, 6H); 4.70 and 4.43 (two br s, 2H); 3.08 and 2.89 (two br s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05916891 |
| Source dataset | uspto-grants-1999_06 |
| ORD ID | ord-1ff28bfc3e584cef8a18dbece02cb89a |
| Source note | uspto-grants-1999_06 |