HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 14307920, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Iodide Ion | HCID 30165 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 22842949 | HCID 22842949 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 14307920 | HCID 14307920 | — |
Reaction Steps
Methyl iodide (7.9 ml) is added to a solution of 16α-methylandrosta-4,9(11)-dien-3-one 17β-carboxylate (7.9 g) and diisopropylethylamine (17.5 ml) in acetonitrile (175 ml). The mixture is allowed to stand at 20°-25° for 2 hr and then a second addition of amine (9 ml) and iodide (4 ml) is made. The mixture is allowed to stand overnight at 20°-25° and then concentrated under reduced pressure. The residue is partitioned (water and methylene chloride) and the extract is concentrated and chromatographed on silica gel (750 g). Elution is performed with acetone/methylene chloride (2-5%/98-95%). The appropriate fractions are pooled and concentrated to give the title compound, m.p. 127.5° (acetone-hexane)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05380840 |
| Source dataset | uspto-grants-1995_01 |
| ORD ID | ord-cb7f140c722743c4a4fb66e497ecd9c1 |
| Source note | uspto-grants-1995_01 |