HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 18472580, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 18472507 | HCID 18472507 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 18472580 | HCID 18472580 | — |
Reaction Steps
A solution of 7—(4-methylphenyl)-2-phenyl-N-(4—(piperidinomethyl)phenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (0. 08 g) and methyl iodide (0.05 ml) in dimethylformamide (15 ml) was stirred at room temperature overnight. The solvent was evaporated, and to the residue was added ethyl acetate. Precipitated crude crystal was filtered, which were recrystallized from ethanol-ethyl acetate to give 1—(N-(7—(4-methylphenyl)-2-phenyl-2,3-dihydro-1-benzoxepin-4-carbonyl)-4-aminobenzyl)-1-methylpiperidinium iodide (Compound 103) (0.057 g) as colorless crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413947B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-6d288f988a1b45588ca0dedad4a01d4a |
| Source note | uspto-grants-2002_07 |