HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 77750436, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | HCID 77750365 | HCID 77750365 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 77750436 | HCID 77750436 | — |
Reaction Steps
Sodium hydride (65.3 mg) was added to a solution of the diol from step (b) (1.23 g) and methyl iodide (0.13 ml) in DMF (4 ml) and the mixture was stirred for 4 h. Ammonium chloride solution was added and the mixture was extracted with ethyl acetate. The organic extracts were dried, concentrated and purified (SiO2, petrol:acetone 4:1 and petrol:ethyl acetate 2:1 as eluants) to give the subtitle compound (676 mg) as a 1:2.5 mixture with the regioisomeric [1R-[1α,2α,3β,5β(1R*,2S*)]]-3-[7-[N-(2,4-dimethoxyphenylmethyl)-(2-phenylcyclopropyl)amino]]-5-propylthio-3H-1,2,3-triazolo[4,5d]pyrimidin-3-yl]-5-[[[(1,1-dimethylethyl)diphenylsilyl]oxy]methyl]-2-methoxycyclopentanol compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06251910B1 |
| Source dataset | uspto-grants-2001_06 |
| ORD ID | ord-628f7ef851094814b91acf13e53527e8 |
| Source note | uspto-grants-2001_06 |