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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182679Generated: October 31, 2026

Sodium borohydride → HCID 20786230, compound

https://huagongshe.com/reaction/2182679

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 numberUS06897224B2
Source datasetuspto-grants-2005_05
ORD IDord-d85e1b2ff01f43f8a0b66b4499bc0459
Source noteuspto-grants-2005_05