Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 86699220 | HCID 86699220 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 71816083 | HCID 71816083 | 90% |
Reaction Steps
5-(3,5-Dichloro-benzoyl)-5,6-dihydro-cyclopenta[b]thiophen-4-one (1.5 g, 4.8 mmol), hydrazine monohydrate (0.35 mL, 7.2 mmol), glacial acetic acid (0.8 mL) and ethanol (15 mL) were heated at 100° C. under nitrogen for 4 hr. The mixture was cooled to 25° C. and concentrated under reduced pressure to give a solid which was recrystallized from ethanol to provide the corresponding 6-(3,5-Dichloro-phenyl)-4,7-dihydro-1-thia-4,5-diaza-cyclopenta[a]pentalene (1.33 g, 4.3 mmol) as yellow solid in 90% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853207B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-f235181dea6d4c11904146ab2f1e4cf6 |
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| Source note | uspto-grants-2014_10 |
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