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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377972Generated: October 30, 2026

Sodium borohydride → HCID 22915648, compound

https://huagongshe.com/reaction/1377972

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86749172HCID 86749172—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22915648HCID 22915648—

Reaction Steps

65.5 mg (0.126 mmol) of methyl 6-[(2-butyl-4-chloro-5-formyl-1H-imidazol-1-yl)methyl]-2-(2-methoxycarbonyl-phenyl-4-quinolinecarboxylate obtained in Example 5 were dissolved in a mixed solvent of 2 ml of tetrahydrofuran and 2 ml of methanol and the mixture was stirred. After adding 5.24 mg (0.139 mmol) of sodium borohydride, the reaction mixture was allowed to react at room temperature for one hour. Then, the reaction mixture was concentrated under reduced pressure and dichloromethane was added to the residue followed by washing with a saturated sodium chloride solution. The organic layer was dried over magnesium sulfate and filtered. The filtrate was concentrated under reduced pressure to obtain 50.6 mg of methyl 6-[(2-butyl-4-chloro-5-hydroxymethyl-1H-imidazol-1-yl)methyl]-2-(2-methoxycarbonyl-phenyl)-4-quinolinecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665881
Source datasetuspto-grants-1997_09
ORD IDord-608415ddfd154282b9c16421cedb004a
Source noteuspto-grants-1997_09