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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1671655Generated: October 31, 2026

Sodium borohydride → HCID 178477644, compound

https://huagongshe.com/reaction/1671655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 178477645HCID 178477645—
SolventMethanolHCID 887—
ProductHCID 178477644HCID 178477644—

Reaction Conditions

Temperature60 °C

Reaction Steps

Sodium borohydride (15 mg) was added to a methanol (1 ml) solution of methyl (6-(4-(ethylsulfonyl)phenoxy)-2-pyridin-2-yl-1H-benzimidazol-5-yl)(hydroxy)acetate (21 mg) obtained in Example 31 (step 2), and the reaction liquid was stirred overnight at 60° C. The solvent was evaporated away under reduced pressure, and the reaction mixture was purified through reversed-phase middle-pressure liquid chromatography (ODS-AS-360-CC (by YMC), mobile phase: water/acetonitrile/0.1% trifluoroacetic acid), and the resulting fraction was diluted with ethyl acetate, washed with aqueous saturated sodium bicarbonate and saturated saline water in that order, and dried with anhydrous sodium sulfate. The solvent was evaporated away under reduced pressure to obtain the entitled compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994331B2
Source datasetuspto-grants-2011_08
ORD IDord-6360223bbebe479d943468311ec7796c
Source noteuspto-grants-2011_08