HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylhomopiperazine → HCID 13656993, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylhomopiperazine | HCID 228349 | — |
| Reactant | HCID 13656984 | HCID 13656984 | — |
| Product | HCID 13656993 | HCID 13656993 | 69.7% |
Reaction Steps
In the same manner as described in Example 3, N-methylhomopiperazine (2.6 g) and 2-chloromethyl-1-(2-ethoxyethyl)benzimidazole (2.38 g) obtained in the same manner as described in Reference Example 3 are reacted to give 1-(2-ethoxyethyl)-2-(4-methyl-1-homopiperazinyl)methylbenzimidazole (2.2 g) as a pale yellow liquid. This liquid is treated with fumaric acid (1.63 g), and the crude crystal thus obtained is recrystallized from a mixed solvent of ethyl acetate-ethanol to give 1-(2-ethoxyethyl)-2-(4-methyl-1-homopiperazinyl)methylbenzimidazole 3/2 fumarate semihydrate (2.2 g) as colorless prisms, m.p. 119°-121.5° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04603130 |
| Source dataset | uspto-grants-1986_07 |
| ORD ID | ord-50170243cead4b0d962a80f51e210c0b |
| Source note | uspto-grants-1986_07 |