HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,8-Diazabicyclo(5.4.0)undec-7-ene → (2R,5S)-4-(4-Cyano-3-methoxyphenyl)-2,5-dimethyl-N-(6-trifluoromethyl-3-pyridyl)piperazine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,8-Diazabicyclo(5.4.0)undec-7-ene | HCID 81184 | — |
| Reactant | Methyl [6-(trifluoromethyl)pyridin-3-yl]carbamate | HCID 23082060 | — |
| Reactant | 4-[(2S,5R)-2,5-dimethylpiperazin-1-yl]-2-methoxybenzonitrile | HCID 68691204 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | (2R,5S)-4-(4-Cyano-3-methoxyphenyl)-2,5-dimethyl-N-(6-trifluoromethyl-3-pyridyl)piperazine-1-carboxamide | HCID 10320641 | 45.7% |
Reaction Conditions
| Temperature | 100 °C |
|---|
Reaction Steps
Into 5 ml of toluene were dissolved 500 mg of methyl 6-(trifluoromethyl)pyridin-3-ylcarbamate and 557 mg of 4-[(2S,5R)-2,5-dimethylpiperazin-1-yl]-2-methoxybenzonitrile, and then 0.03 ml of DBU was added thereto, followed by heating to 100° C. and 8 hours of stirring. The reaction solution was concentrated and the residue was subjected to silica gel column chromatography to obtain 450 mg of the title compound from an eluate using chloroform-methanol (96:4, v/v).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07666873B2 |
| Source dataset | uspto-grants-2010_02 |
| ORD ID | ord-badd1e69609b43b8aafcfe4aa0d69adc |
| Source note | uspto-grants-2010_02 |