HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,2,2-Trichloroethanimidamide → HCID 178516502, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,2,2-Trichloroethanimidamide | HCID 35608 | — |
| Reactant | Acetoacetate | HCID 6971017 | — |
| Reactant | Pyrimidinyl carbamate | HCID 54270844 | — |
| Product | HCID 178516502 | HCID 178516502 | — |
Reaction Steps
The pyrimidinyl carbamate compounds of the present invention may be prepared by reacting trichloroacetamidine with the corresponding acetoacetate to form the corresponding 4-hydroxy-2-trichloromethylpyrimidine, which is then reacted with a selected carbamoyl chloride. These general reactions are illustrated below in equations (A) and (B). In equation (A), trichloroacetamidine is reacted with methylacetoacetate to form 4-hydroxy-6-methyl-2-trichloromethylpyrimidine. In equation (B), the 4-hydroxy-6-methyl-2-trichloromethylpyrimidine is reacted with dimethylcarbamoyl chloride to form 6-methyl-2-trichloromethyl-4-pyrimidinyl dimethylcarbamate. ##STR3##
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04343803 |
| Source dataset | uspto-grants-1982_08 |
| ORD ID | ord-fa375f70ac0e4887b51c5e9492a4cc48 |
| Source note | uspto-grants-1982_08 |