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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1386731Generated: October 26, 2026

4-Hydroxy-4-(3-(3,5-difluoro-4-hydroxyphenyl)propyl)piperidine → 2-(r)-(3-(s)-((4-Hydroxy-4-(3-(3,5-difluoro-4-hydroxyphenyl)prop-1-yl)piperidin-1-yl)methyl)-4-(s)-phenylpyrrolidin-1-yl)-2-(cyclohexyl)acetic acid

https://huagongshe.com/reaction/1386731

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydroxy-4-(3-(3,5-difluoro-4-hydroxyphenyl)propyl)piperidineHCID 21180661—
Reactant2-(R)-(3-(R)-formyl-4-(S)-phenylpyrrolidin-1-yl)-2-(cyclohexyl)acetic acid, benzyl esterHCID 59924617—
Product2-(r)-(3-(s)-((4-Hydroxy-4-(3-(3,5-difluoro-4-hydroxyphenyl)prop-1-yl)piperidin-1-yl)methyl)-4-(s)-phenylpyrrolidin-1-yl)-2-(cyclohexyl)acetic acidHCID 20672408—

Reaction Steps

The title compound was prepared from 2-(R)-(3-(R)-formyl-4-(S)-phenylpyrrolidin-1-yl)-2-(cyclohexyl)acetic acid, benzyl ester (from EXAMPLE 1, Step I) and 4-hydroxy-4-(3-(3,5-difluoro-4-hydroxyphenyl) propyl)piperidine.HCl (from EXAMPLE 83, Step B) using procedures analogous to those described in EXAMPLE 71, Steps A and B. For the title compound: 1H NMR (500 MHz) 8 0.95-3.42 (35H), 5.16 (ABq, J=12.0, 2H), 6.56 (d, J=8.0, 2H), 7.21-7.30 (5H); ESI-MS 571 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06265434B1
Source datasetuspto-grants-2001_07
ORD IDord-858d581364d047daac9344ae0d9c39cf
Source noteuspto-grants-2001_07