HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Methylpiperazine → HCID 15345718, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Methylpiperazine | HCID 53167 | — |
| Reactant | HCID 19419847 | HCID 19419847 | — |
| Product | HCID 15345718 | HCID 15345718 | 57% |
Reaction Steps
A solution of 7-bromo-2-chloro-5,6-dihydro-4H-imidazo[4,5,1-ij]quinoline (3.00 g) in N-methylpiperazine (20 ml) was stirred under reflux, under nitrogen, for two hrs. The reaction mixture was quenched with dilute sodium bicarbonate solution (200 ml) and extracted with chloroform. The combined organic extracts were dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was purified by high performance liquid chromatography (silica gel; 7:1 dichloromethane-methanol). The appropriate fractions were collected and evaporated. The residue was recrystallized from ethyl acetate-ether to give 2.1 g (57%) of product, mp 132°-133° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05563272 |
| Source dataset | uspto-grants-1996_10 |
| ORD ID | ord-7f17b67110bc40968aaa746cf6be8a05 |
| Source note | uspto-grants-1996_10 |