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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2260557Generated: November 2, 2026

Sodium borohydride → HCID 22915648, compound

https://huagongshe.com/reaction/2260557

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86749172HCID 86749172—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22915648HCID 22915648153.9%

Reaction Steps

65.5 mg (0.126 mmol) of methyl 6-[(2-butyl-4-chloro-5-formyl-1H-imidazol-1-yl)methyl]-2-(2-methoxycarbonylphenyl)-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-methoxycarbonylphenyl)-4-quinolinecarboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05478832
Source datasetuspto-grants-1995_12
ORD IDord-fa46c22c68234398b51b072c7604922d
Source noteuspto-grants-1995_12