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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2054959Generated: October 30, 2026

Sodium borohydride → HCID 20786230, compound

https://huagongshe.com/reaction/2054959

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 69203328HCID 69203328—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 20786230HCID 20786230—

Reaction Steps

703 mg (1.47 mmol) of 8-[4-(5-fluoro-2-methoxyphenyl)-2-hydroxy-4-methyl-2-trifluoromethyl-pentylidenamino]quinoline-2-carboxylic acid amide in 10 ml of methanol and 5.0 ml of tetrahydrofuran are mixed with 449 mg (11.8 mmol) of sodium borohydride. After 16 hours, the solvent is concentrated by evaporation, the residue is taken up in water and ethyl acetate, extracted with ethyl acetate, and the combined organic phases are dried on sodium sulfate. After removal of the solvent and purification on silica gel with hexane-ethyl acetate (0-50%) as well as dichloromethane-methanol (0-7%), 358 mg (51% of-theory) of the product is obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07329753B2
Source datasetuspto-grants-2008_02
ORD IDord-1393919044b647f4bf2ebb8608a8d1b9
Source noteuspto-grants-2008_02