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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 221989Generated: October 30, 2026

Sodium borohydride → HCID 44556080, compound

https://huagongshe.com/reaction/221989

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant2,2,2-trifluoro-N-(3-oxo-1-{-4-[9-phenyl-3-(2-pyrimidinyl)[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8-yl]phenyl}cyclobutyl)acetamideHCID 58229853—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 44556080HCID 44556080—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a mixture of 2,2,2-trifluoro-N-(3-oxo-1-{4-[9-phenyl-3-(2-pyrimidinyl)[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8-yl]phenyl}cyclobutyl)acetamide (4-2) (25 mg, 0.043 mmol) in CH2Cl2 (1 mL) and MeOH (1 mL) was added NaBH4 (2.0 mg, 0.052 mmol) at −78° C., and the mixture was stirred at −78° C. for 1 hour. The mixture was quenched with sat. NH4Cl, extracted with CHCl3, washed with brine, dried (MgSO4), filtered, and concentrated under reduced pressure to give 2,2,2-trifluoro-N-(3-hydroxy-1-{-4-[9-phenyl-3-(2-pyrimidinyl)[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8-yl]phenyl}cyclobutyl)acetamide (4-3). MS (M+H)+: observed=581, calculated=581.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207169B2
Source datasetuspto-grants-2012_06
ORD IDord-f25060e5892a4a5685309d8d781f06dc
Source noteuspto-grants-2012_06