HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → 6-Chloro-9-isopropyl-9h-purin-2-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 6-chloro-1H-purin-2-amine | HCID 178508435 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Chloro-9-isopropyl-9h-purin-2-amine | HCID 21933771 | — |
Reaction Steps
To 6-chloro-9H-purin-2-ylamine (20 g, 0.12 moles) in DMF (200 mL) at −11° C. was added NaH (5.7 g, 0.14 moles, 60%) portionwise over 1 h. The mixture as stirred for 1 h, then 2-iodopropane (14.2 mL, 0.14 moles) was added dropwise. The solution was warmed to rt, stirred for 18 h, quenched with sat'd NH4Cl, and extracted with EtOAc. The combined extracts, were washed with water, sat'd NaCl, then dried over MgSO4 and filtered. Concentration yielded an oil which was purified by silica gel chromatography (60% EtOAc/Hexane) to a white solid (13.4 g, 54%): MS [M+H]+ 212; m.p. 135–136° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07115589B2 |
| Source dataset | uspto-grants-2006_10 |
| ORD ID | ord-5aadb1613e1f4cee91ad470aa1b97597 |
| Source note | uspto-grants-2006_10 |