HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1778449Generated: November 1, 2026
HCID 90003329, compound → HCID 123167069, compound
https://huagongshe.com/reaction/1778449
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 90003329 | HCID 90003329 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 123167069 | HCID 123167069 | — |
Reaction Steps
The (2S,6R)-tert-butyl 4-(5-((R)-3-(4-amino-3-(2-fluoro-4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidin-1-yl)-4-cyano-2-methyl-5-oxopent-3-en-2-yl)-2,6-dimethylpiperazine-1-carboxylate (103.5 mg, 0.1400 mmol) was dissolved in 4N HCl in dioxane, and stirred at rt for 3 hours. The solvent was removed and 2 mL of MeOH was added to the residues. The mixture was neutralized to pH around 7-8 and extracted with DCM. The combined organic layer was washed with brine, dried over sodium sulfate, filtered, and the solvent evaporated to get pure product 2-((R)-3-(4-amino-3-(2-fluoro-4-phenoxyphenyl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)piperidine-1-carbonyl)-4-((3S,5R)-3,5-dimethylpiperazin-1-yl)-4-methylpent-2-enenitrile as a white solid. MS (pos. ion) m/z: 638 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09266895B2 |
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| Source dataset | uspto-grants-2016_02 |
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| ORD ID | ord-23187f1e98ae49d8abe5b059c849e7d6 |
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| Source note | uspto-grants-2016_02 |
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