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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1881698Generated: November 1, 2026

(S)-2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidin-2-yl)methoxy)acetic acid → 2-[[(2S)-1-[(4-Methoxy-2,6-dimethyl-phenyl)sulfonyl]-piperidin-2-yl]-methoxy]-1-[4-pyridin-3-yl-4-[2-(1H-[1,2,4]triazol-1-yl)-ethoxy]-piperidin-1-yl]-ethanone

https://huagongshe.com/reaction/1881698

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidin-2-yl)methoxy)acetic acidHCID 57819715—
Reactanttert-butyl 4-(2-(1H-1,2,4-triazol-1-yl)ethoxy)-4-(pyridin-3-yl)piperidine-1-carboxylateHCID 57916248—
Product2-[[(2S)-1-[(4-Methoxy-2,6-dimethyl-phenyl)sulfonyl]-piperidin-2-yl]-methoxy]-1-[4-pyridin-3-yl-4-[2-(1H-[1,2,4]triazol-1-yl)-ethoxy]-piperidin-1-yl]-ethanoneHCID 4446588624%

Reaction Steps

The desired target compound was synthesized under reaction conditions analogously to the process described for Example 61 (see below) from (S)-2-((1-(4-methoxy-2,6-dimethylphenylsulfonyl)piperidin-2-yl)methoxy)acetic acid [acid D] and tert-butyl 4-(2-(1H-1,2,4-triazol-1-yl)ethoxy)-4-(pyridin-3-yl)piperidine-1-carboxylate [amine G]. Yield: 24%. MS, Rt=3.3 min, m/z=627.4 [MH]+

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08318769B2
Source datasetuspto-grants-2012_11
ORD IDord-eee110a1897842ce9ed06e48cbd4a7b6
Source noteuspto-grants-2012_11