HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(4-methyl-4H-1,2,4-triazol-3-yl)phenyl]pyrimidine-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-(4-Methyl-4H-1,2,4-Triazol-3-Yl)Aniline | HCID 2794785 | — |
| Reactant | 6-[Cyclohexyl(cyclopropylmethyl)amino]pyrimidine-4-carboxylic acid | HCID 59446841 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-[cyclohexyl(cyclopropylmethyl)amino]-N-[4-(4-methyl-4H-1,2,4-triazol-3-yl)phenyl]pyrimidine-4-carboxamide | HCID 59446877 | — |
Reaction Steps
A solution of 6-(cyclohexyl(cyclopropylmethyl)amino)pyrimidine-4-carboxylic acid (Intermediate 13, 100 mg; 0.36 mmol) in DCM (4 ml) was treated with polymer-supported Mukaiyama reagent (400 mg) followed by triethylamine (100 mL; 0.73 mmol) and 4-(4-methyl-4H-1,2,4-triazol-3-yl)aniline (Maybridge, 63.2 mg; 0.36 mmol). After stirring at RT for 24 hours the mixture was filtered and washed with saturated sodium bicarbonate solution. The organic phase was passed through a hydrophobic frit and the solvent removed in vacuo. The residue was purified by column chromatography (silica) eluting with petroleum ether containing increasing amounts of EtOAc to give the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08399448B2 |
| Source dataset | uspto-grants-2013_03 |
| ORD ID | ord-062f0a141cb44ef3a97746284294455b |
| Source note | uspto-grants-2013_03 |