Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl 2-hydrazinyl-2-oxoacetate | HCID 2786935 | — |
| Reactant | Ethyl {2-cyano-1-[4-(trifluoromethyl)phenyl]ethenyl}carbamate | HCID 76754610 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178470152 | HCID 178470152 | — |
Reaction Steps
2.4 g (8.4 mmol) of ethyl {2-cyano-1-[4-(trifluoromethyl)phenyl]ethenyl}carbamate (Example 129A) and 1.24 g (8.4 mmol) of ethyl hydrazino(oxo)acetate are dissolved in NMP (16 ml) and stirred in a flask with a calcium chloride drying tube at an oil-bath temperature of 160° C. for 4 h. The reaction mixture is cooled to RT and poured into water (100 ml), and the precipitate is filtered off, washed with water and diethyl ether and dried. 1.90 g (64% of theory) of the crude product are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08273752B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-8c8e4702971a441ebee9f3752d2f4477 |
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| Source note | uspto-grants-2012_09 |
|---|