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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 429688Generated: October 30, 2026

Sodium borohydride → HCID 86757594, compound

https://huagongshe.com/reaction/429688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 86757595HCID 86757595—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 86757594HCID 86757594464.3%

Reaction Steps

To a solution of 3-methoxy-N-methyl-N-[4-methyl-2-[5-(4-oxopiperidin-1-yl)carbonylpent-1-yloxy]phenyl]-4-[2-(tert-butoxycarbonyl)aminomethyl-1H-benzimidazol-4-yl]-carbonylaminobenzamide (150 mg) in methanol (5 ml) was added sodium borohydride (7.52 mg) under an ice bath cooling and the mixture was stirred at the same temperature for 1 hour. The mixture was diluted with chloroform and the solution was washed with water and brine. The organic phase was dried over magnesium sulfate and the solvent was evaporated in vacuo to give N-[2-[5-(4-hydroxypiperidin-1-yl)carbonylpent-1-yloxy]-4-methylphenyl]-3-methoxy-N-methyl-4-[2-tert-butoxycarbonyl)aminomethyl-1H-benzimidazol-4-yl]carbonylaminobenzamide (150 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06316482B1
Source datasetuspto-grants-2001_11
ORD IDord-eefa20fac9144a40b448469307f83df7
Source noteuspto-grants-2001_11