HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75687Generated: November 1, 2026
Sodium triacetoxyborohydride → HCID 67234529, compound
https://huagongshe.com/reaction/75687
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | N-Benzyl-2-azabicyclo[2.2.1]heptan-7-one | HCID 49759181 | — |
| Reactant | HCID 66716091 | HCID 66716091 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 67234529 | HCID 67234529 | 25% |
Reaction Steps
To a solution of 1-(5-amino-1H-indazol-1-yl)-2,2-dimethylpropan-1-one maleate salt (580 mg, 1.7 mmol, prepared as described in U.S. Ser. No. 08/021,4614) and 2-benzyl-2-azabicyclo[2.2.1]heptan-7-one (250 mg, 1.7 mmol) (J. R. Malpass, S. Handa, and R. White, Org. Lett., 2005, 7, 2759-2762) in THF (9 mL) was added sodium triacetoxyborohydride (740 mg, 3.5 mmol), and the mixture was stirred at ambient temperature for 24 h. The reaction mixture was partitioned between aqueous sodium bicarbonate and ethyl acetate, and the organic layer was washed with brine and dried over sodium sulfate. The solvent was evaporated and the residue was purified by normal phase chromatography followed by reversed phase HPLC to afford 175 mg (25%) of 1-(5-((1SR,4SR,7RS)-2-benzyl-2-azabicyclo[2.2.1]heptan-7-ylamino)-1H-indazol-1-yl)-2,2-dimethylpropan-1-one.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08835457B2 |
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| Source dataset | uspto-grants-2014_09 |
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| ORD ID | ord-83bc017d7f1942caafe96998ef1adcd1 |
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| Source note | uspto-grants-2014_09 |
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