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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1278751Generated: October 29, 2026

4-((2S)-3-Amino-2-hydroxy-propoxy)-phenol → N-Benzyl-4-{4-[(2S)-2-hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-piperidin-1-yl}-benzenesulfonamide

https://huagongshe.com/reaction/1278751

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((2S)-3-Amino-2-hydroxy-propoxy)-phenolHCID 9877547—
ReactantN-benzyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamideHCID 12051788—
ProductN-Benzyl-4-{4-[(2S)-2-hydroxy-3-(4-hydroxy-phenoxy)-propylamino]-piperidin-1-yl}-benzenesulfonamideHCID 10301195—

Reaction Steps

The title compound was prepared from 4-((2S)-3-Amino-2-hydroxy-propoxy)-phenol and Reference Example 70, N-benzyl-4-(4-oxo-piperidin-1-yl)-benzenesulfonamide, according to the procedure of Example 1 as a tan solid. 1H NMR (DMSO) δ 1.27 (m, 2H), 1.86 (m, 2H), 2.75(m, 3H), 2.91(t, 2H, J=8.4 Hz), 3.82(m, 5H), 3.89(s, 2H), 4.89(m, 1H), 6.67 (d, J=6.6 Hz), 6.76(d, 2H, J=6.6 Hz), 7.02 (d, 2H, J=6.6 Hz), 7.26 (m, 5H), 7.57 (d, 2H, J=6.6 Hz), 7.78)bs, 1H), 8.87(bs, 1H); MS (ES) m/z: 512.1 (MH+); HRMS for C27H33N3O5S: 511.2215 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06444685B1
Source datasetuspto-grants-2002_09
ORD IDord-015942dbbe074847b9108e0e9bd6c720
Source noteuspto-grants-2002_09