HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Allylcyclohexylamine → N-Allyl-N-cyclohexyl-2-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-3-methylisonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Allylcyclohexylamine | HCID 81115 | — |
| Reactant | 2-[4-(3,3-Diphenyl-1-propyl)piperazin-1-yl]-3-methylisonicotinic acid | HCID 22180513 | — |
| Product | N-Allyl-N-cyclohexyl-2-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-3-methylisonicotinamide | HCID 22180238 | 68.1% |
Reaction Steps
Step (d) of Example 107 was repeated, except that the compound (50 mg) prepared in step (c) of Example 109 and allylcyclohexylamine (34 mg) were used as the starting compounds. Thus, the title compound (44 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030120B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-d7332c65ab8547bfbf7efe6f6ceb66e0 |
| Source note | uspto-grants-2006_04 |