HuagongsheHuagongshe Chemistry Print Report · For research reference only
Thionyl Chloride → n-(3,5-Bis trifluoromethyl-benzyl)-n-cyclopropyl-4-o-tolyl-nicotinamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Thionyl Chloride | HCID 24386 | — |
| Reactant | 4-(2-Methylphenyl)nicotinic acid | HCID 15887406 | — |
| Reactant | (3,5-Bistrifluoromethylbenzyl)cyclopropylamine | HCID 15887407 | — |
| Catalyst | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | n-(3,5-Bis trifluoromethyl-benzyl)-n-cyclopropyl-4-o-tolyl-nicotinamide | HCID 9806536 | 58.5% |
Reaction Steps
A solution of 106 mg (0.5 mmol) 4-o-tolyl-nicotinic acid in 5 ml dichloromethane and 2 drops N,N-dimethylformamide was stirred with 0.1 ml (1.4 mmol) thionyl chloride for 1.5 h at room temperature. The solvent was removed and the residue was taken up in 5 ml dichloromethane and 0.3 ml triethylamine. After the addition of 155 mg (0.55 mmol) (3,5-bis-trifluoromethyl-benzyl)-cyclopropyl-amine the mixture was stirred at room temperature for 1 h and washed twice with water. The organic layer was dried (magnesium sulfate) and evaporated. The crude oil was subjected to column chromatography to give 140 mg (58%) of the title compound as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06297375B1 |
| Source dataset | uspto-grants-2001_10 |
| ORD ID | ord-5d5120a0398f4c2dbae2f4f6d6fdd56e |
| Source note | uspto-grants-2001_10 |