HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → 2-Isopropylamino-6-methyl-pyrimidine-4-carbonitrile
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 2-Isopropylamino-6-methyl-pyrimidine-4-carboxylic acid amide | HCID 68509301 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Isopropylamino-6-methyl-pyrimidine-4-carbonitrile | HCID 68508217 | 249.2% |
Reaction Steps
To a suspension of 2-isopropylamino-6-methyl-pyrimidine-4-carboxylic acid amide (1.24 g, 6.4 mmol) in DCM (20 mL), pyridine (2.53 mL, 25.6 mmol) is added followed by TFFA (2.7 mL, 19.2 mmol). The reaction mixture is stirred for 4 h, and then is quenched with water. The mixture is extracted with DCM. The org. phase is washed with sat. aq. NaHCO3 and dried over MgSO4, filtered and evaporated. Purification by CC on silica gel (eluting with Heptane/EtOAc 4:1) affords the 2-isopropylamino-6-methyl-pyrimidine-4-carbonitrile as a yellow oil (2.81 g); LC-MS: tR=0.89; [M+H]+=177.04.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08299086B2 |
| Source dataset | uspto-grants-2012_10 |
| ORD ID | ord-13eae6f1fb91407c9a1179df01e6dc6b |
| Source note | uspto-grants-2012_10 |