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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061402Generated: November 1, 2026

(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamide → HCID 69654864, compound

https://huagongshe.com/reaction/1061402

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-N-(5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl)methanesulfonamideHCID 12047933—
ReactantHCID 69655037HCID 69655037—
ProductHCID 69654864HCID 69654864—

Reaction Steps

The title compound was prepared from 3-[4-(4-oxo-piperidine-1-yl)-phenylsulfamoyl]-thiophene-2-carboxylic acid methyl ester (which was obtained in Example 234) and N-[5-((1R)-2-amino-1-hydroxy-ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 10) according to the procedure of Example 278 as a pale yellowish solid; 1H NMR (300 MHz, DMSO-d6) δ 1.20-1.40 (m, 2H), 1.70-1.90 (m, 2H), 2.50-2.75 (m, 5H), 3.40-3.55 (m, 2H), 3.89 (s, 2H), 4.46 (dd, J=8.0, 4.2 Hz, 1H), 6.75-6.85 (m, 3H), 6.90 (d, J=9.0 Hz, 2H), 7.00 (dd, J=8.3, 2.0 Hz, 1H), 7.16 (d, J=2.0 Hz, 1H), 7.32 (d, J=3.3 Hz, 1H), 7.89 (d, J=3.3 Hz, 1H); MS (ES) m/z: 624.9 (MH+); HRMS Calcd. for C26H34N4O8S3 (MH+): 625.1455. Found: 625.1441.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-5b2bf803f8ff4a428d263ccbcd49b28a
Source noteuspto-grants-2003_02