Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | HCID 54502621 | HCID 54502621 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 19699129 | HCID 19699129 | — |
Reaction Steps
To a mixture of 2.2 g of 7-[(dimethyl-amino)methylene]-4,5,6,7-tetrahydro-4-(2-chloro-4-nitrobenzoyl)-8H-thieno[3,2-b]azepine in 40 ml of ethanol is added 341 μl of hydrazine followed by heating at 60° C. for 1.5 hours. The volatiles are evaporated in vacuo to a residue which is dissolved in 100 ml of ethyl acetate and filtered through a pad of hydrous magnesium silicate. The filtrate is evaporated in vacuo to give 1.85 g of the desired product as a yellow-orange solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05719278 |
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| Source dataset | uspto-grants-1998_02 |
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| ORD ID | ord-baac543988d3410daca6dc1f0398bc66 |
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| Source note | uspto-grants-1998_02 |
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