HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzoyl chloride → Aniline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzoyl chloride | HCID 7412 | — |
| Reactant | HCID 15908598 | HCID 15908598 | — |
| Reactant | HCID 178523892 | HCID 178523892 | — |
| Product | Aniline | HCID 6115 | — |
| Product | Benzhydrylamine | HCID 7036 | — |
Reaction Steps
N-[1-(2,4-Dichlorophenyl)-2-(imidazol-1-yl)-ethyl]-N′-phenyl)carbonyl thiourea. Compound A was prepared by following the procedure of Example 190, Step A, except benzoyl chloride was used instead of 4-chlorobenzoyl chloride. B. N-[1-(2,4-Dichlorophenyl)-2-(imidazol-1-yl)-ethyl]—N′-phenyl-N″-phenylcarbonylguanidine. Step B of Example 190 was followed using Compound A, above, and aniline (instead of diphenylmethylamine) to obtain Example 191. MS (ES): m/z 478 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06916813B2 |
| Source dataset | uspto-grants-2005_07 |
| ORD ID | ord-49ab3c0fb15146ed8515e83e9d9d940f |
| Source note | uspto-grants-2005_07 |