HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-Allylcyclohexylamine → N-Allyl-N-cyclohexyl-2-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-5-methylisonicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-Allylcyclohexylamine | HCID 81115 | — |
| Reactant | 2-[4-(3,3-Diphenyl-1-propyl)piperazin-1-yl]-5-methylisonicotinic acid | HCID 22180640 | — |
| Product | N-Allyl-N-cyclohexyl-2-[4-(3,3-diphenyl-1-propyl)piperazin-1-yl]-5-methylisonicotinamide | HCID 22180511 | 72.8% |
Reaction Steps
Step (d) of Example 107 was repeated, except that the compound (50 mg) prepared in step (d) of Example 108 and allylcyclohexylamine (34 mg) were used as the starting compounds. Thus, the title compound (47 mg) was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07030120B2 |
| Source dataset | uspto-grants-2006_04 |
| ORD ID | ord-8e757de0a427484089bebbeffbfb2f9f |
| Source note | uspto-grants-2006_04 |