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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2188282Generated: October 29, 2026

4-((2S)-3-Amino-2-hydroxy-propoxy)-phenol → HCID 178518026, compound

https://huagongshe.com/reaction/2188282

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-((2S)-3-Amino-2-hydroxy-propoxy)-phenolHCID 9877547—
ReactantHCID 178516398HCID 178516398—
ProductHCID 178518026HCID 178518026—

Reaction Steps

The title compound was prepared from 1-{4-[2-(1-benzyl-piperdin-4-ylamino)-4-oxo-4H-thiazol-5-ylidenemethyl]-phenyl}-piperidin-4-one (which was obtained in Intermediate 21) and 4-[(2S)-3-amino-2-hydroxy-propoxyl]-phenol (which was obtained in Intermediate 5) according to the procedure of Example 1 as a pale yellowish solid; mp>175° C. (dec.); 1H NMR (300 MHz, DMSO-d6) δ1.20-1.40 (m, 2 H), 1.40-1.65 (m, 2 H), 1.70-2.00 (m, 4 H), 2.06 (brt, J=9.5 Hz, 2 H), 2.55-2.95 (m, 6 H), 3.47 (s, 2 H), 3.70-4.00 (m, 5 H), 4.92 (brs, 1 H), 6.66 (d, J=6.8 Hz, 2 H), 6.75 (d, J=6.8 Hz, 2 H), 7.02 (d, J=9.0 Hz, 2 H), 7.20-7.50 (m, 8 H), 8.89 (brs, 1 H), 9.29 (brs, 1 H); MS (ES) m/z:321.6 ((M+2H)2+, 100%); 642.1 (MH+, 5%); HRMS Calcd. for C36H44N5O4S (MH+): 642.3114. Found: 642.3095.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06410734B1
Source datasetuspto-grants-2002_06
ORD IDord-a2d4232ce725491b81ca7972b234c3ab
Source noteuspto-grants-2002_06