Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Stannous Chloride | HCID 24479 | — |
| Reactant | HCID 19699129 | HCID 19699129 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19699078 | HCID 19699078 | 93.6% |
Reaction Steps
A mixture of 1.8 g of 6-(2-chloro-4-nitrobenzoyl)-1,4,5,6-tetrahydropyrazolo[3,4-d]thieno[3,2-b]azepine in 35 ml of absolute ethanol is added 5.42 g of tin (II) chloride followed by heating at reflux for 1 hour at 80° C. The volatiles are evaporated in vacuo to a residue which is partitioned between 150 ml of ethyl acetate and saturated aqueous NaHCO3 the reactants are stirred at room temperature for 1 hour and filtered. The organic layer is separated and washed with 30 ml of brine, dried (Na2SO4) and filtered through a pad of hydrous magnesium silicate. The filtrate is evaporated in vacuo to give 1.55 g of a yellow-orange foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05532235 |
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| Source dataset | uspto-grants-1996_07 |
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| ORD ID | ord-2f11e1defaee4ba3b14992360926cff3 |
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| Source note | uspto-grants-1996_07 |
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