HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 10747204, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | HCID 10626473 | HCID 10626473 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10747204 | HCID 10747204 | — |
Reaction Steps
A solution of 2—(4-piperidinophenyl)-N-(4—((N-tetrahydropyran-4-yl-N-methylamino)methyl)phenyl)-6,7-dihydro-5H-benzocycloheptene-8-carboxamide (0.2 g) and methyl iodide (0.025 ml) in dimethylformamide (10 ml) was stirred at room temperature over night. The solvent was evaporated, and the residue was purified with silica gel column (chloroform/methanol) to give crude crystals, which were recrystallized from ethanol-hexane to give dimethyl-(N-(2—(4-piperidinophenyl)-6,7-dihydro-5H-benzocyclo-heptene-8-carbonyl)-4-aminobenzyl)-4-tetrahydropyranyl-ammonium iodide (Compound 225) (0.15 g) as pale brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06413947B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-48addbda068e47d599c824a9c1df993e |
| Source note | uspto-grants-2002_07 |