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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 570570Generated: October 29, 2026

2-(4-(3-(4-Chlorophenyl)-1,2,4-thiadiazol-5-yl)piperazin-1-yl)-1-(4-methoxyphenyl)ethanol → 2-{4-[3-(4-Chloro-phenyl)-[1,2,4]thiadiazol-5-yl]-piperazin-1-yl}-1-(3-methoxy-phenyl)-ethanol

https://huagongshe.com/reaction/570570

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(4-(3-(4-Chlorophenyl)-1,2,4-thiadiazol-5-yl)piperazin-1-yl)-1-(4-methoxyphenyl)ethanolHCID 71186574—
Reactant2-{4-[3-(4-Chloro-phenyl)-[1,2,4]thiadiazol-5-yl]-piperazin-1-yl}-1-(3-methoxy-phenyl)-ethanoneHCID 71187302—
Product2-{4-[3-(4-Chloro-phenyl)-[1,2,4]thiadiazol-5-yl]-piperazin-1-yl}-1-(3-methoxy-phenyl)-ethanolHCID 71186397—

Reaction Steps

In analogy to the procedure described for the synthesis of 2-{4-[3-(4-Chloro-phenyl)-[1,2,4]thiadiazol-5-yl]-piperazin-1-yl}-1-(4-methoxy-phenyl)-ethanol (Example 54) the title compounds was prepared from 2-{4-[3-(4-Chloro-phenyl)-[1,2,4]thiadiazol-5-yl]-piperazin-1-yl}-1-(3-methoxy-phenyl)-ethanone through reduction as white solid. MS (m/e): 431.3 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09023852B2
Source datasetuspto-grants-2015_05
ORD IDord-48bb0bf82efa470dbb9a2ac18aab3651
Source noteuspto-grants-2015_05