Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351711Generated: October 27, 2026

(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide → N-[2-Hydroxy-5-(1-hydroxy-2-{1-[4-(toluene-4-sulfonyl)-phenyl]-piperidin-4-ylamino}-ethyl)-phenyl]-methanesulfonamide

https://huagongshe.com/reaction/351711

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
Reactant1-[4-(Toluene-4-sulfonyl)-phenyl]-piperidin-4-oneHCID 22713358—
ProductN-[2-Hydroxy-5-(1-hydroxy-2-{1-[4-(toluene-4-sulfonyl)-phenyl]-piperidin-4-ylamino}-ethyl)-phenyl]-methanesulfonamideHCID 10281140—

Reaction Steps

The title compound was prepared according to the procedure of Example 1 from 0.13 g (0.4 mmol) of Reference Example 25, 1-[4-(Toluene-4-sulfonyl)-phenyl]-piperidin-4-one, and 0.12 g (0.5 mmol) of (R)-N-[5-(2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl}-methanesulfonamide, yielding 0.18 g of a white solid; m.p. 115-118° C.; MS (ES) m/z 560.0 (MH+); HRMS (FAB) Calcd. for C27H34N3O6S2 (MH+): 560.1889, Found: 560.1886.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743787B2
Source datasetuspto-grants-2004_06
ORD IDord-45aab5adea28444da76aaa8b98e2677c
Source noteuspto-grants-2004_06