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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1901353Generated: November 2, 2026

Citric Acid → 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(6-cyano-2-indolyl)propanol

https://huagongshe.com/reaction/1901353

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCitric AcidHCID 311—
ReactantMethanolHCID 887—
ReactantSodium borohydrideHCID 4311764—
ReactantHCID 56998289HCID 56998289—
SolventTetrahydrofuranHCID 8028—
Product2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(6-cyano-2-indolyl)propanolHCID 5702933386.4%

Reaction Steps

2.7 g of methyl 2-[4-[((3S)-1-tert-butoxycarbonyl-3-pyrrolidinyl)oxy]phenyl]-3-(6-cyano-2-indolyl)propionate was dissolved in 30 ml of tetrahydrofuran, followed by the addition of 660 mg of sodium borohydride. 12 ml of methanol was added dropwise to the thus prepared solution while stirring under ice cooling, and the resulting mixture was stirred at room temperature for 3 hours. The resulting reaction solution was mixed with 10% citric acid aqueous solution, extracted with dichloromethane, and then dried. After distilling off the solvent, the resulting residue was purified by subjecting it to silica gel column chromatography using a dichloromethane/methanol mixture as an elution solvent. In this way, 2.2 g of the title compound was obtained in an oily form.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05576343
Source datasetuspto-grants-1996_11
ORD IDord-2365062be1104b54a94ddbd4a898f42c
Source noteuspto-grants-1996_11