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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061387Generated: November 2, 2026

4-((2S)-3-Amino-2-hydroxy-propoxy)-phenol → N-[4-(4-{[(2S)-2-Hydroxy-3-(4-hydroxyphenoxy)propyl]amino}-1-piperidineyl)phenyl]-5-{[5-(trifluoromethyl)-2-pyridinyl]sulfonyl}-2-thiophenesulfonamide

https://huagongshe.com/reaction/1061387

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((2S)-3-Amino-2-hydroxy-propoxy)-phenolHCID 9877547—
Reactant5-(5-Trifluoromethyl-pyridin-2-sulfonyl)-thiophene-2-sulfonic acid [4-(4-oxo-piperidin-1-yl)-phenyl]-amideHCID 86584571—
ProductN-[4-(4-{[(2S)-2-Hydroxy-3-(4-hydroxyphenoxy)propyl]amino}-1-piperidineyl)phenyl]-5-{[5-(trifluoromethyl)-2-pyridinyl]sulfonyl}-2-thiophenesulfonamideHCID 69654929—

Reaction Steps

The title compound was prepared from 5-(5-trifluoromethyl-pyridine-2-sulfonyl)-thiophene-2-sulfonic acid [4-(4-oxo-piperidine-1-yl)-phenyl]-amide (which was obtained in Example 229) and 4-((2S)-3-amino-2-hydroxy-propoxyl)-phenol (which was obtained in Example 5) according to the procedure of Example 278 as a grey solid; 1H NMR (300 MHz, DMSO-d6) δ 1.25-1.45 (m, 2H), 1.70-1.95 (m, 2H), 2.50-2.85 (m, 5H), 3.54 (brd, J=12.4 Hz, 2H), 3.65-3.95 (m, 3H), 6.60-6.90 (m, 8H), 7.92 (d, J=1.6 Hz, 1H), 8.41 (d, J=8.3 Hz, 1H), 8.48 (d, J=1.6 Hz, 1H), 8.61 (dd, J=8.3, 2.0 Hz, 1H), 8.89 (s, 1H), 9.23 (s, 1H); MS (ES) m/z: 713.1 (MH+); HRMS Calcd. for C30H32F3N4O7 S3 (MH+): 713.1385. Found: 713.1407.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525202B2
Source datasetuspto-grants-2003_02
ORD IDord-4954b5a0f5e642b0bc6d6048ea096bc5
Source noteuspto-grants-2003_02