Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 13245578 | HCID 13245578 | — |
| Reactant | HCID 53775369 | HCID 53775369 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13240342 | HCID 13240342 | 51.9% |
Reaction Steps
0.24 g (10 mmole) of sodium hydride was suspended in 10 ml of N,N-dimethylformamide, to which was added 2.45 g (12 mmole) of 3-(3,4-methylenedioxyphenyl)-5-pyrazolone with stirring at room temperature. After evolution of hydrogen had ceased, to this solution was added dropwise 10 ml of a solution of 5.87 g (10 mmole) of 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-methoxycarbonylpyridine-5-carboxylic acid 6-tosyloxyhexyl ester in N,N-dimethylformamide, and the mixture was stirred and heated at 90° C. for an hour. The resultant reaction mixture was poured into 200 ml of ice water, and the separated solid was filtered off. This solid was recrystallized from ethyl acetate to obtain 3.21 g (yield 51.9%) of the 1,4-dihydro-2,6-dimethyl-4-(3-nitrophenyl)-3-methoxycarbonylpyridine-5-carboxylic acid 6-[5-(3,4-methylenedioxyphenyl)-3-pyrazolyloxy]hexyl ester.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04418197 |
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| Source dataset | uspto-grants-1983_11 |
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| ORD ID | ord-ffc755195b3240b08bb2a1366c847ac9 |
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| Source note | uspto-grants-1983_11 |
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