HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → (R)-2,6-dichloro-5-methyl-N-(tetrahydrofuran-3-yl)pyrimidin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2,4,6-Trichloro-5-methylpyrimidine | HCID 232789 | — |
| Reactant | (3R)-3-Aminotetrahydrofuran hydrochloride | HCID 46856371 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | (R)-2,6-dichloro-5-methyl-N-(tetrahydrofuran-3-yl)pyrimidin-4-amine | HCID 90426233 | 54.8% |
Reaction Steps
A mixture of 2,4,6-trichloro-5-methylpyrimidine (2 g, 10.2 mmol), (R)-tetrahydrofuran-3-amine hydrochloride (1.12 g, 9.2 mmol) and Et3N (2.1 g, 20.3 mmol) in EtOH (20 mL) was stirred at room temperature for 14 h., concentrated under vacuum and the residue was purified by chromatographic column on silica gel (EtOAc/petroleum ether, gradient elution, from 1/0 to 2/1) to give the (R)-2,6-dichloro-5-methyl-N-(tetrahydrofuran-3-yl)pyrimidin-4-amine (1.25 g, 53% yield) as a white solid. ESI-LCMS (m/z): 248.1 [M+1]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09346802B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-772f106915e948ccb144b2c781f961a0 |
| Source note | uspto-grants-2016_05 |