HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Allylcyclohexylamine → n-Allyl-n-cyclohexyl-5-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-2-isopropylbenzamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Allylcyclohexylamine | HCID 81115 | — |
| Reactant | 2-Fluoro-5-nitrobenzoic acid | HCID 280997 | — |
| Reactant | n-Allyl-n-cyclohexyl-5-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-2-fluorobenzamide | HCID 22180389 | — |
| Product | n-Allyl-n-cyclohexyl-5-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-2-isopropylbenzamide | HCID 22180348 | — |
Reaction Steps
Steps (a) and (b) of Example 59 were repeated, except that the compound prepared just above in step (a) was used instead of 2-fluoro-5-nitrobenzoic acid. Step (d) of Example 1 was then repeated, except that N-allylcyclohexylamine was used instead of N-methylbenzylamine. Thus, the title compound was prepared.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030120B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-c81ce5498cca4b658ec1b00d9bacf2ba |
| Source note | uspto-grants-2006_04 |