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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1348560Generated: November 1, 2026

Sodium borohydride → HCID 11657239, compound

https://huagongshe.com/reaction/1348560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 21091639HCID 21091639—
SolventMethanolHCID 887—
SolventSodium chloride; waterHCID 57417360—
ProductHCID 11657239HCID 1165723968.2%

Reaction Steps

To a mixture of 15 mg (0.41 mmol) sodium borohydride in 2 ml methanol were added at 0° C. 200 mg (0.338 mmol) 2-(3,5-bis-trifluoromethyl-phenyl)-N-[4-(2-formyl-phenyl)-6-(4-methyl-piperazin-1-yl)-pyridin-3-yl]-N-methyl-isobutyramide. After stirring at 0° C. for 1 h 1 ml brine was added at 0° C. The mixture was stirred for 30 min. Methanol was distilled off and the residue was diluted with 20 ml ethyl acetate and washed with 20 ml brine. The organic layer was dried over sodium sulfate, concentrated and purified by flash chromatography to give 137 mg (68%) of the title compound as a light brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07211579B2
Source datasetuspto-grants-2007_05
ORD IDord-3fa8f07b29844bf59d1eb19e2e2c9e6f
Source noteuspto-grants-2007_05