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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 351709Generated: October 27, 2026

(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide → [Butyl-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylamino-phenyl)-ethylamino]-piperidin-1-yl}-benzenesulfonyl)-amino]-acetic acid ethyl ester

https://huagongshe.com/reaction/351709

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
Reactant{Butyl-[4-(4-oxo-piperidin-1-yl)-benzenesulfonyl]-amino}-acetic acid ethyl esterHCID 69899530—
Product[Butyl-(4-{4-[(2R)-2-hydroxy-2-(4-hydroxy-3-methanesulfonylamino-phenyl)-ethylamino]-piperidin-1-yl}-benzenesulfonyl)-amino]-acetic acid ethyl esterHCID 69900453—

Reaction Steps

The title compound was prepared according to the procedure of Example 1 from 1.03 g (2.6 mmol) of Reference Example 43, {butyl-[4-(4-oxo-piperidin-1-yl)-benzenesulfonyl]-amino}-acetic acid ethyl ester, and 0.77 g (3.1 mmol) of (R)-N-[5-(2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl}-methanesulfonamide, yielding 1.05 g of a light yellow solid; m.p. 94-95° C.; MS (ES) m/z 627.2 (MH+); HRMS (ES) Calcd. for C28H43N4O8S2 (MH+): 627.2517, Found: 627.2505.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06743787B2
Source datasetuspto-grants-2004_06
ORD IDord-e2ead0a1b7f443cd9f92adcad48cc5b9
Source noteuspto-grants-2004_06