HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzenemethanol, 2,6-dichloro- → 1-(2-Butenyl)-7-(2,6-dichlorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzenemethanol, 2,6-dichloro- | HCID 27156 | — |
| Reactant | 1-(2-Butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine | HCID 53719624 | — |
| Product | 1-(2-Butenyl)-7-(2,6-dichlorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine | HCID 54503552 | 83.5% |
Reaction Steps
The title compound (cis/trans=21:79) was prepared as a pale yellow powder in 83.5% yield in a similar procedure to that described in Example 1 by using 1-(2-butenyl)-7-chloro-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=24/76) and 2,6-dichlorobenzyl alcohol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063782 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-a1fa01ac0e87449c974144d55ba80d6c |
| Source note | uspto-grants-2000_05 |