HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzylamine → 3-Benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzylamine | HCID 7504 | — |
| Reactant | 3-Chloro-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine | HCID 19385500 | — |
| Product | 3-Benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine | HCID 19385483 | 92.4% |
Reaction Steps
14 g (46 mmol) of 3-chloro-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine are heated in 74 g (0.69 mol) of benzylamine at 200° C. for 3 hours. The mixture is subsequently poured onto ice and extracted with dichloromethane, and the organic phase is dried with potassium carbonate and then concentrated. Petroleum ether (b.p. 50°-70° C.) is added to the residue, and the resulting precipitate is filtered off with suction and crystallized from ethyl acetate/cyclohexane. 15.9 g (92.4%) of 3-benzylamino-6-(3-cyclopentyloxy-4-methoxyphenyl)pyridazine of m.p. 116° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05449676 |
| Source dataset | uspto-grants-1995_09 |
| ORD ID | ord-9d574a73ca0645858722c352ff47eb81 |
| Source note | uspto-grants-1995_09 |