HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → HCID 66885794, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | HCID 11978818 | HCID 11978818 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Reactant | HCID 66885795 | HCID 66885795 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 66885794 | HCID 66885794 | — |
Reaction Steps
By a similar method as in Example 18, 7-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-2-ethyl-3,4-dihydro-2H-isoquinolin-1-one was prepared from 7-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-3,4-dihydro-2H-isoquinolin-1-one using ethyl iodide, and after it was made into a methanol solution, 0.5N hydrochloric acid methanol solution was added thereto, precipitated crystals were separated by filtration, recrystallized from a mixed solvent of methanol-ethyl acetate and thereby 7-[3-(4-benzo[b]thiophen-4-yl-piperazin-1-yl)propoxy]-2-ethyl-3,4-dihydro-2H-isoquinolin-1-one dihydrochloride 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-c16d363395244eb488aabc7ab27d7534 |
| Source note | uspto-grants-2013_01 |