HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465507Generated: November 2, 2026
Hydrazine hydrate (1:1) → HCID 58181225, compound
https://huagongshe.com/reaction/1465507
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1,1'-Carbonyldiimidazole | HCID 68263 | — |
| Reactant | HCID 58181239 | HCID 58181239 | — |
| Reactant | HCID 67030329 | HCID 67030329 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 58181225 | HCID 58181225 | 85.9% |
Reaction Steps
To a solution of 3-(4-{2-[5-(4-acetylpiperazin-1-yl)pyridin-2-yl]ethyl}thiophen-2-yl)propan-1-ol (150.0 mg, 0.402 mmol) in anhydrous tetrahydrofuran (3 ml) was added 1,1′-carbonyldiimidazole (84.7 mg, 0.522 mmol), and the mixture was stirred at room temperature for 2 hrs. 1M Hydrazine tetrahydrofuran solution (1.21 ml, 1.21 mmol) was added, and the mixture was stirred at room temperature for 2 hrs. Since the reaction did not proceed, hydrazine monohydrate (26.1 mg, 0.522 mmol) was added, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure, and the residue was purified by aminopropylated silica gel column chromatography (5%-2-propanol-dichloromethane mixture) and aminopropylated silica gel column chromatography (2%-methanol-dichloromethane mixture) to give the title compound (148.8 mg, yield 85.9%) as a colorless syrup.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08999989B2 |
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| Source dataset | uspto-grants-2015_04 |
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| ORD ID | ord-04c1036c1e854e6392634e83e490949d |
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| Source note | uspto-grants-2015_04 |
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