HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl Isocyanate → HCID 22004635, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl Isocyanate | HCID 12228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 22004591 | HCID 22004591 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 22004635 | HCID 22004635 | 71.3% |
Reaction Steps
A solution of 3-{benzyl-[6-methyl-3-methylsulfanyl-1-(2,4,6-trichlorophenyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl]amino}-propan-1-ol (100 mg, 0.191 mmol) in 2 ml of dry THF was treated with 6 mg of 60% sodium hydride in oil and methyl isocyanate (39 mg, 6.78 mmol) at room temperature and stirred at room temperature for 10 hours. The mixture was quenched with water and extracted with ethyl acetate. The organic layer was dried and concentrated to give 110 mg of white form. The form was purified through silica gel column chromatography to give 79 mg of the title compound as a white glass form. 1H NMR (CDCl3): 2.03(m,2H), 2.51(s,3H), 2.59(s,3H), 2.77(d,3H), 3.79(t,2H), 4.12(t,2H), 4.50(brs,1H), 5.17(s,2H), 7.2-7.45(m,5H), 7.51(s,2H)ppm.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06218397B1 |
| Source dataset | uspto-grants-2001_04 |
| ORD ID | ord-492c6f93fd104c81835e4b2b4704a329 |
| Source note | uspto-grants-2001_04 |