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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1071653Generated: November 2, 2026

4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexanol → 1-[4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexyl]-4-[2-(3-cyanophenoxy)ethyl]piperazine

https://huagongshe.com/reaction/1071653

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexanolHCID 22393645—
Reactant1-(3-Cyanophenoxyethyl)piperazineHCID 22393683—
Reactant[4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexyloxy]-tert-butyldimethylsilaneHCID 22393724—
Reactant1-[4-Cyano-5-methyl-4-(3-thienyl)hexyl]-4-[2-(3-fluorophenoxy)ethyl]piperazineHCID 22393737—
Product1-[4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexyl]-4-[2-(3-cyanophenoxy)ethyl]piperazineHCID 22393588—

Reaction Steps

By using [4-cyano-5-methyl-4-(2-bromo-5-thienyl)hexyloxy]-tert-butyldimethylsilane (700 mg) which was obtained in Example 114-5) described in JP-A 11-206862, 4-cyano-5-methyl-4-(2-bromo-5-thienyl)hexanol (371 mg, 80%) was synthesized as a yellow oil in accordance with Example 114-8) described in JP-A 11-206862. From 105 mg of the resulting compound and 96 mg of 2-(3-cyanophenoxy)ethylpiperazine, the title compound was synthesized as a colorless oil in accordance with the production method described in Example 84 (138 mg, 62%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06906072B1
Source datasetuspto-grants-2005_06
ORD IDord-35f6c561fb04432faff3cb177622ccc0
Source noteuspto-grants-2005_06