Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Ethyl 3-(4-chlorophenyl)-3-oxopropanoate | HCID 101336 | — |
| Reactant | 2-Hydrazinylpyridine-4-carbonitrile | HCID 20118714 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178510212 | HCID 178510212 | 76.6% |
Reaction Steps
To a mixture of ethyl 3-(4-chlorophenyl)-3-oxopropanoate (500 mg, 2.2 mmol) and 2-hydrazinylpyridine-4-carbonitrile (PREPARATION 2, 296 mg, 2.2 mmol) in EtOH (15 mL) was added AcOH (2 mL) at r.t. The reaction mixture was stirred at 90° C. overnight. After the reaction was completed, the mixture was concentrated, washed with PE/EA (10 mL, V/V=1/1) to give the title compound (500 mg, 76%) as a brown solid and used as crude for next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09107916B2 |
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| Source dataset | uspto-grants-2015_08 |
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| ORD ID | ord-6a446636a9cb43da9ea02f67e1bfed31 |
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| Source note | uspto-grants-2015_08 |
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