HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Chloroethyl chloroformate → N-[4-(1,2,3,6-tetrahydro-4-pyridinyl)phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Chloroethyl chloroformate | HCID 521305 | — |
| Reactant | N-[4-[1,2,3,6-tetrahydro-1-(phenylmethyl)-4-pyridinyl]phenyl]-4'-(trifluoromethyl)-[1,1'-biphenyl]-2-carboxamide | HCID 22499387 | — |
| Solvent | 1,2-Dichloroethane | HCID 11 | — |
| Product | N-[4-(1,2,3,6-tetrahydro-4-pyridinyl)phenyl]-4'-(trifluoro-methyl)-[1,1'-biphenyl]-2-carboxamide | HCID 22499395 | 126.2% |
Reaction Steps
1-Chloroethyl chloroformate (0.078 mol) was added dropwise to a stirring mixture of intermediate (20) (0.039 mol) in 1,2-dichloro-ethane (500 ml). The mixture was stirred for 30 minutes and then stirred and refluxed overnight. The solvent was evaporated. Methanol (500 ml) was added. The mixture was stirred and refluxed overnight. The solvent was evaporated. The residue was triturated in DIPE. The precipitate was filtered off and dried, yielding 20.8 g of N-[4-(1,2,3,6-tetrahydro-4-pyridinyl)phenyl]-4′-(trifluoro-methyl )-[1,1′-biphenyl]-2-carboxamide (intermediate 21).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07169796B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-644646099f2f46b186fda1e8baa8895f |
| Source note | uspto-grants-2007_01 |