HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methyl iodide → HCID 66885614, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Ethanol hydrochloride | HCID 21887872 | — |
| Reactant | HCID 66885604 | HCID 66885604 | — |
| Reactant | HCID 66885615 | HCID 66885615 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 66885614 | HCID 66885614 | — |
Reaction Steps
By a similar method as in Example 18, 6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-2-methyl-2H-isoquinolin-1-one was prepared from 6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-2H-isoquinolin-1-one using methyl iodide, and after it was made into an ethyl acetate solution, 1N hydrochloric acid ethanol solution was added thereto, precipitated crystals were separated by filtration, recrystallized from ethyl acetate and thereby 6-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-2-methyl-2H-isoquinolin-1-one hydrochloride was obtained in the form of a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08349840B2 |
| Source dataset | uspto-grants-2013_01 |
| ORD ID | ord-a9713004ea8d441a9d8de98b388321d4 |
| Source note | uspto-grants-2013_01 |