HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 21715701, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 18472465 | HCID 18472465 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 21715701 | HCID 21715701 | — |
Reaction Steps
A solution of 7-(4-piperidinophenyl)-N-(4-((N-tetrahydropyran-4-yl-N-methylamino)methyl)phenyl)-2,3-dihydro-1-benzoxepine-4-carboxamide (0.2 g) and methyl iodide (0.025 ml) in dimethylformamide (5 ml) was stirred at room temperature over night. 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 dimethyl(N-(7-(4-piperidinophenyl)-2,3-dihydro-1-benzoxepin-4-carbonyl)-4-aminobenzyl)-4-tetrahydropyranylammonium iodide (Compound 221) (0.1 g) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06166006 |
| Source dataset | uspto-grants-2000_12 |
| ORD ID | ord-147a5f6e600049fb9eee47f661c5d9fa |
| Source note | uspto-grants-2000_12 |