HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1093207Generated: October 31, 2026
HCID 66589115, compound → 4-(4-((1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)-1-(2,2,2-trifluoroethyl)-1H-pyrazolo[3,4-d]pyrimidin-6-yl)aniline
https://huagongshe.com/reaction/1093207
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 66589115 | HCID 66589115 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 4-(4-((1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)-1-(2,2,2-trifluoroethyl)-1H-pyrazolo[3,4-d]pyrimidin-6-yl)aniline | HCID 66589046 | 93.9% |
Reaction Steps
A suspension of (1R,4R)-5-(6-(4-nitrophenyl)-1-(2,2,2-trifluoroethyl)-1H-pyrazolo[3,4-d]pyrimidin-4-yl)-2-oxa-5-azabicyclo[2.2.1]heptane (0.50 g, 1.2 mmol) in tetrahydrofuran (20 mL) and water (5 mL) was degassed by the addition of crushed dry ice and then treated with 10% palladium on carbon (50 mg). The resulting suspension was evacuated under weak vacuum and then filled with hydrogen gas (balloon). This evacuation/fill cycle was performed three more times and on the final iteration, the mixture was left to stir overnight under a hydrogen filled balloon. The mixture was filtered through a pad of diatomaceous earth, eluting with methanol. The filtrate was concentrated under reduced pressure to afford 4-(4-((1R,4R)-2-oxa-5-azabicyclo[2.2.1]heptan-5-yl)-1-(2,2,2-trifluoroethyl)-1H-pyrazolo[3,4-d]pyrimidin-6-yl)aniline as a gray foam (0.44 g, 93%). MS (ES+): 391.2 (M+H)+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08129371B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-7cc40e2edb614b2290010bdb7f95272b |
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| Source note | uspto-grants-2012_03 |
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