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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 618705Generated: October 29, 2026

Sodium borohydride → HCID 9910284, compound

https://huagongshe.com/reaction/618705

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantChloroform methanolHCID 21584188—
ReactantHCID 21847959HCID 21847959—
SolventMethanolHCID 887—
ProductHCID 9910284HCID 9910284—

Reaction Steps

200 mg (0.47 mmol) of 5-((5-(2-oxo-2-(2-phenyl-5-methyl-4-oxazolyl)ethoxy)-2-pyridyl)methyl)thiazolidin-2,4-dione (Compound No. I-2a-1) was dissolved in 5 ml of methanol dehydrated with molecular sieve. To this solution, was added 21.5 mg of sodium borohydride, and the resultant solution was stirred at room temperature for 1 day. The reaction was terminated with a saturated aqueous solution of ammonium chloride, and the reaction mixture was extracted with chloroform. The reaction product thus obtained was washed with brine, and was dried over anhydrous magnesium sulfate. After removing the drying agent by filtration, the solvent was distilled off under a reduced pressure to obtain a residue, and the residue thus obtained was subjected to silica gel column chromatography (eluent: 10%--methanol/chloroform) to obtain 203 mg (quantitative) of pale brown powder of the aimed product (Compound No. I-2a-3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05955481
Source datasetuspto-grants-1999_09
ORD IDord-db842186d78549d6a88406b69899a655
Source noteuspto-grants-1999_09