HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 10555236, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | HCID 10646694 | HCID 10646694 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 10555236 | HCID 10555236 | — |
Reaction Steps
To a solution of N-[4-(1-piperidinylmethyl)phenyl]-6-(4-methylphenyl)-2 H-1-benzopyran-3-carboxamide (200 mg) in DMF (3 ml) was added methyl iodide (0.1 ml) at room temperature, and the mixture was stirred for 20 hours. To the mixture was added ethyl acetate. Precipitated crystal was collected by filtration and recrystallized from chloroform-ethanol to give 1-[4-[N-[6-(4-methylphenyl)2 H-1-benzopyran-3-carbonyl]-amino]benzyl]-1-methyl-piperidinium iodide (Compound 198) (188 mg) as yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06172061B2 |
| Source dataset | uspto-grants-2001_01 |
| ORD ID | ord-2ed46a3f453847c4978a9413fd0603b0 |
| Source note | uspto-grants-2001_01 |