Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methylhydrazine | HCID 6061 | — |
| Reactant | HCID 54520283 | HCID 54520283 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19607529 | HCID 19607529 | 72.1% |
Reaction Steps
4.53 mL (0.085 mol) of methyl hydrazine (purchased from Aldrich Chemical Company) was added dropwise to a mixture of 21.54 g (0.066 mol) of the title compound of Step D in 115 mL of ethanol. The mixture was stirred at reflux under nitrogen for 5 hr and was then evaporated to dryness. The crude product was chromatographed over silica gel eluting with a mixture of (1:9) ethyl acetate:hexane to yield two components. Concentration of the major fraction yielded 14.72 g of the title compound of Step E as an oil; 1H NMR (CDCl3): δ2.3 (s,3H), 2.82 (s,3H), 3.76 (s,2H), 3.9 (s,3H), 7.2 (s, 1H), 7.3 (s,1H). Concentration of the minor fraction yielded 3.87 g of the isomer 8-bromo-1,4-dihydro-1,6,9-trimethyl[1]benzothiopyrano[4,3-c]pyrazole as an oil; 1H NMR (CDCl3): δ2.3 (s,3H), 2.46 (s,3H), 3.75 (s,3H), 3.59 and 3.81 (2d,2H), 7.4 (s,1H), 7.45 (s,1H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05985799 |
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| Source dataset | uspto-grants-1999_11 |
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| ORD ID | ord-680fc627ed4c4b19b94940ba65217e1f |
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| Source note | uspto-grants-1999_11 |
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