HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 67339653, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 67338376 | HCID 67338376 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 67339653 | HCID 67339653 | 731.3% |
Reaction Steps
Add sodium hydride (0.78 g, 1.9 mmol, 60% in mineral oil) to 1,2,4,5-tetrahydro-6H-[1,4]diazepino[6,7,1-hi]indol-7-one (3.05 g, 1.62 mmol) in dry dimethylformamide (77 mL). Stir for 30 minutes at room temperature and then add iodomethane (2.0 mL, 3.2 mmol). Stir at room temperature for 134 minutes. Partition between ethyl acetate (1 L) and water (500 mL). Wash the organic phase with saturated aqueous sodium chloride, dry over sodium sulfate, and concentrate under reduced pressure. Subject the residue to chromatography (pre-packed silica gel), eluting with a gradient: 1:0-9:1 ethyl acetate/methanol to provide the desired compound (2.42 g, 74%) as an off-white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08022065B2 |
| Source dataset | uspto-grants-2011_09 |
| ORD ID | ord-d6d636926d3144cf9471ce707cd34723 |
| Source note | uspto-grants-2011_09 |