HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → 5-chloro-N4-(6-methoxyhexahydrofuro[3,2-b]furan-3-yl)-N2-(1-methyl-1H-pyrazol-4-yl)pyrimidine-2,4-diamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-methyl-1H-pyrazol-4-amine | HCID 17354268 | — |
| Reactant | 2,5-dichloro-N-(6-methoxyhexahydrofuro[3,2-b]furan-3-yl)pyrimidin-4-amine | HCID 118387991 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 5-chloro-N4-(6-methoxyhexahydrofuro[3,2-b]furan-3-yl)-N2-(1-methyl-1H-pyrazol-4-yl)pyrimidine-2,4-diamine | HCID 118387953 | 42.7% |
Reaction Steps
A solution of 2,5-dichloro-N-(6-methoxyhexahydrofuro[3,2-b]furan-3-yl)pyrimidin-4-amine (430 mg, 1.4046 mmol), DIPEA (546.7 mg, 4.23 mmol) and 1-methylpyrazol-4-amine hydrochloride (283.3 mg, 2.12 mmol) in n-BuOH (10 mL) was stirred in a sealed tube at 150° C. for 23 h. The reaction solution was concentrated in vacuo, and the residue was purified by silica gel column chromatography (DCM/MeOH (v/v)=50/1) to give the crude product as a white solid. The crude product was recrystallized from acetone to give the title compound as a white solid (220 mg, 42.6%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09394281B2 |
| Source dataset | uspto-grants-2016_07 |
| ORD ID | ord-1a64800943d04ad6853b380969613849 |
| Source note | uspto-grants-2016_07 |