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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1533812Generated: November 4, 2026

Sodium borohydride → HCID 18355175, compound

https://huagongshe.com/reaction/1533812

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 18354977HCID 18354977—
SolventMethanolHCID 887—
SolventChloroformHCID 6212—
ProductHCID 18355175HCID 1835517599.7%

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 numberUS06207693B1
Source datasetuspto-grants-2001_03
ORD IDord-cc227f6815ac41ff9b5066ffea1a29a0
Source noteuspto-grants-2001_03