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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061314Generated: November 4, 2026

N-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamide → HCID 10210215, compound

https://huagongshe.com/reaction/1061314

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-[5-(2-amino-1-hydroxyethyl)-2-hydroxyphenyl]methanesulphonamideHCID 9837752—
ReactantHCID 69654958HCID 69654958—
ProductHCID 10210215HCID 10210215—

Reaction Steps

The title compound was prepared from 2-[4-(4-oxo-piperidine-1-yl)-benzylidene]-malonic acid diethyl ester (which was obtained in Example 153) and N-[5-(-2-amino-1-hydroxy- ethyl)-2-hydroxy-phenyl]-methanesulfonamide (which was obtained in Example 9) according to the procedure of Example 180 as a yellowish solid; mp >80° C. (decomposed); 1H NMR (300 MHz, DMSO-d6) δ 1.21 (t, J=7.0 Hz, 3H), 1.23 (t, J=7.0 Hz, 3H), 1.75-1.95 (m, 2H), 2.50-3.50 (m, 7H), 2.92 (s, 3H), 3.75-3.90 (m, 2H), 4.21 (q, J=7.0 Hz, 2H), 4.31 (q, J=7.0 Hz, 2H), 4.47 (dd, J=8.0, 4.2 Hz, 1H), 6.81 (d, J=8.2 Hz, 1H), 6.94 (d, J=9.0 Hz, 2H), 7.00 (dd, J=8.2, 2.0 Hz, 1H), 7.17 (d, J=2.0 Hz, 1H), 7.33 (d, J=9.0 Hz, 2H), 7.52 (s, 1H); MS (ES) m/z: 576.1 (MH+); HRMS Calcd. for C28H38N3O8S(MH+): 576.2374. Found: 576.2375.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-2d6b5103831e46c991ba613ab6962e80
Source noteuspto-grants-2003_02