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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 58181239HCID 58181239—
ReactantHCID 67030329HCID 67030329—
SolventTetrahydrofuranHCID 8028—
ProductHCID 58181225HCID 5818122585.9%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08999989B2
Source datasetuspto-grants-2015_04
ORD IDord-04c1036c1e854e6392634e83e490949d
Source noteuspto-grants-2015_04