HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl 2,6-difluorobenzene-1-carboximidate → ethyl N-[4-(3-chloro-5-trifluoromethylpyrid-2-yloxy)-3,5-dichlorophenylcarbamoyl]-2,6-difluorobenzimidate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl 2,6-difluorobenzene-1-carboximidate | HCID 13730259 | — |
| Reactant | 3-Chloro-2-(2,6-dichloro-4-isocyanatophenoxy)-5-(trifluoromethyl)pyridine | HCID 13913613 | — |
| Product | ethyl N-[4-(3-chloro-5-trifluoromethylpyrid-2-yloxy)-3,5-dichlorophenylcarbamoyl]-2,6-difluorobenzimidate | HCID 54449738 | — |
Reaction Steps
In a similar manner to that described in step (e) of Example I ethyl 2,6-difluorobenzimidate is reacted with 3-chloro-5-trifluoromethyl-2-(2,6-dichloro-4-isocyanatophenoxy)pyridine to give ethyl N-[4-(3-chloro-5-trifluoromethylpyrid-2-yloxy)-3,5-dichlorophenylcarbamoyl]-2,6-difluorobenzimidate (Compound IV). The intermediate isocyanate is obtained by the procedure of step (c) of Example 1 from 2-(4-amino-2,6-dichlorophenoxy)-3-chloro-5-trifluoromethylpyridine. This compound is described in Japanese published patent application No. 79-125699 (Chemical Abstracts, vol. 92, 146618d).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04559353 |
| Source dataset | uspto-grants-1985_12 |
| ORD ID | ord-602dbcfcced84a2f848be0e8898aadc6 |
| Source note | uspto-grants-1985_12 |