HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine | HCID 53996954 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 1-(2-Butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine hydrochloride | HCID 70105588 | 84.5% |
Reaction Steps
A solution of 0.36 g (0.01 mole) of hydrogen chloride in 3.0 ml of ethanol was added dropwise with ice-cooling to a solution of 2.00 g (0.00615 mole) of 1-(2-butenyl)-7-(4-fluorobenzyloxy)-2,3-dimethylpyrrolo[2,3-d]pyridazine (cis/trans=1/99) in 160 ml of dry diethyl ether and the resulting mixture was stirred at the same temperature for 20 minutes. The reaction mixture was concentrated at room temperature and the residue was washed with a mixture of 10 ml of ethanol and 120 ml of dry diethyl ether. The solid mass thus obtained was then collected by filtration to give 1.88 g of the title compound (trans) as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06063782 |
| Source dataset | uspto-grants-2000_05 |
| ORD ID | ord-a73be3b516fe4667a41837b9fe6eab9d |
| Source note | uspto-grants-2000_05 |