HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl Alcohol → 1-Benzyl-7-benzyloxy-2-methylpyrrolo[2,3-d]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl Alcohol | HCID 244 | — |
| Reactant | 1-Benzyl-7-chloro-2-methylpyrrolo[2,3-d]pyridazine | HCID 19437748 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 1-Benzyl-7-benzyloxy-2-methylpyrrolo[2,3-d]pyridazine | HCID 19437740 | 68% |
Reaction Steps
650 mg (6 mmol) of benzyl alcohol, 10 ml of N-methylpyrrolidone, 1.1 g (10 mmol) of potassium tert-butoxide, 50 mg (0.2 retool) of [18]crown-6 and 500 mg (1.94 retool) of 1-benzyl-7-chloro-2-methylpyrrolo[2,3-d]pyridazine are reacted at room temperature for 2 h. Purification: chromatography on silica gel (eluent: toluene/dioxane=2:1) and crystallization from diisopropyl ether. Yield: 68%, m.p.: 124° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05534515 |
| Source dataset | uspto-grants-1996_07 |
| ORD ID | ord-ff2bbf0a58004ffba39a3770036cd0eb |
| Source note | uspto-grants-1996_07 |