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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260555Generated: November 1, 2026

Sodium borohydride → HCID 22915642, compound

https://huagongshe.com/reaction/2260555

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 15816899HCID 15816899—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22915642HCID 2291564283.2%

Reaction Steps

440 mg (0.953 mmol) of methyl 2-{6-[(2-butyl-4-chloro-5-formyl-1H-imidazol-1-yl)methyl]quinolin-2-yl}benzoate obtained in Example 1 were dissolved in a mixed solvent of 10 ml of tetrahydrofuran and 10 ml of methanol and the mixture was stirred. 40 mg (1.0 mmol) of sodium borohydride were added thereto and allowed to react at room temperature for one hour. After the reaction mixture was concentrated under reduced pressure, dichloromethane was added to the residue and the mixture was washed with a saturated sodium chloride solution. The organic layer was dried over magnesium sulfate followed by filtration. The filtrate was concentrated under reduced pressure to obtain 368 mg of methyl 2-{6-[(2-butyl-4-chloro-5-hydroxymethyl-1H-imidazol-1-yl)methyl]quinolin-2-yl}benzoate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478832
Source datasetuspto-grants-1995_12
ORD IDord-49aea88ac38c4bb1872488af2fc9e4f3
Source noteuspto-grants-1995_12