HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 21163943, compound → Cyano[6-(2-fluorophenoxy)-2-pyridyl]methyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 21163943 | HCID 21163943 | — |
| Reactant | 2-(5-Chloro-2-benzothienyl)-3-methylbutanoic acid | HCID 54204673 | — |
| Reactant | Cyano [6-(3,4-dimethoxyphenyl)-2-pyridyl] methanol | HCID 86737228 | — |
| Product | Cyano[6-(2-fluorophenoxy)-2-pyridyl]methyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate | HCID 53698829 | — |
| Product | 5-Chloro-2-benzothienyl-3-methylbutanoate | HCID 86737227 | — |
Reaction Steps
The alcohol, cyano [6-(3,4-dimethoxyphenyl)-2-pyridyl] methanol and cyano [6-(2-fluorophenoxy)-2-pyridyl]methanol, is reacted with the acid chloride of 2-(5-chloro-2-benzothienyl)-3-methylbutanoic acid to yield cyano[6-(3,4-dimethoxy-phenoxy)-2-pyridyl]methyl 2-(5-chloro-2-benzothienyl-3-methylbutanoate and cyano[6-(2-fluorophenoxy)-2-pyridyl]methyl 2-(5-chloro-2-benzothienyl)-3-methylbutanoate.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04224330 |
| Source dataset | uspto-grants-1980_09 |
| ORD ID | ord-b7f9ee29f1a54a7b8ec9bfa71b21d33a |
| Source note | uspto-grants-1980_09 |