HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 4-(((3S,4S)-4-ethylpyrrolidin-3-yl)amino)-6-(3-methylisoxazol-5-yl)pyrrolo[1,2-b]pyridazine-3-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | (3S,4S)-tert-butyl 3-((3-carbamoyl-6-(3-methylisoxazol-5-yl)pyrrolo[1,2-b]pyridazin-4-yl)amino)-4-ethylpyrrolidine-1-carboxylate | HCID 68291147 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(((3S,4S)-4-ethylpyrrolidin-3-yl)amino)-6-(3-methylisoxazol-5-yl)pyrrolo[1,2-b]pyridazine-3-carboxamide | HCID 68291400 | 107.9% |
Reaction Steps
To a solution of (3S,4S)-tert-butyl 3-((3-carbamoyl-6-(3-methylisoxazol-5-yl)pyrrolo[1,2-b]pyridazin-4-yl)amino)-4-ethylpyrrolidine-1-carboxylate (62 mg, 0.136 mmol) in dichloromethane (1 mL) was added 4N HCl in 1,4-dioxane (0.512 mL, 2.046 mmol). After stirring at room temperature overnight, the deprotection was complete. The volatile were removed in vacuo to afford the hydrochloride salt of the title compound (52 mg, 98% yield) as an off-white solid. MS (ES+) m/z: 355.1 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987268B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-40d01b911c4b42e79168c2adb03901a5 |
| Source note | uspto-grants-2015_03 |