HuagongsheHuagongshe Chemistry Print Report · For research reference only
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
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexanol | HCID 22393645 | — |
| Reactant | 1-(3-Cyanophenoxyethyl)piperazine | HCID 22393683 | — |
| Reactant | [4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexyloxy]-tert-butyldimethylsilane | HCID 22393724 | — |
| Reactant | 1-[4-Cyano-5-methyl-4-(3-thienyl)hexyl]-4-[2-(3-fluorophenoxy)ethyl]piperazine | HCID 22393737 | — |
| Product | 1-[4-Cyano-5-methyl-4-(2-bromo-5-thienyl)hexyl]-4-[2-(3-cyanophenoxy)ethyl]piperazine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06906072B1 |
| Source dataset | uspto-grants-2005_06 |
| ORD ID | ord-35f6c561fb04432faff3cb177622ccc0 |
| Source note | uspto-grants-2005_06 |