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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 75687Generated: November 1, 2026

Sodium triacetoxyborohydride → HCID 67234529, compound

https://huagongshe.com/reaction/75687

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantN-Benzyl-2-azabicyclo[2.2.1]heptan-7-oneHCID 49759181—
ReactantHCID 66716091HCID 66716091—
SolventTetrahydrofuranHCID 8028—
ProductHCID 67234529HCID 6723452925%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08835457B2
Source datasetuspto-grants-2014_09
ORD IDord-83bc017d7f1942caafe96998ef1adcd1
Source noteuspto-grants-2014_09