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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1795005Generated: October 29, 2026

1-Acetylpiperazine → HCID 9960686, compound

https://huagongshe.com/reaction/1795005

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-AcetylpiperazineHCID 83795—
ReactantHCID 22179334HCID 22179334—
SolventWaterHCID 962—
ProductHCID 9960686HCID 996068638%

Reaction Conditions

Temperature150 °C

Reaction Steps

A mixture of 5-[3,5-bis(trifluoromethyl)benzyl]-9-chloro-7-(2-methylphenyl)-6-oxo-2,3,4,5-tetrahydro-6H-pyrido[2,3-b][1,5]oxazocine (compound of Reference Example 17; 100 mg) and 1-acetylpiperazine (73.0 mg) was stirred at 150° C. for 5 hours. To the resulting residue, water was added, and then the mixture was subjected to extraction with ethyl acetate. The resulting extract was dried on anhydrous sodium sulfate. The solvent was removed by distillation to obtain a residue, and then the residue was purified on silica gel column chromatography (ethyl acetate: methanol=10:1) to obtain 9-(4-acetylpiperazine-1-yl)-5-[3,5-bis(trifluoromethyl)benzyl]-7-(2-methylphenyl)-6-oxo-2,3,4,5-tetrahydro-6H-pyrido[2,3-b][1,5]oxazocine (44.6 mg, 38%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07026309B2
Source datasetuspto-grants-2006_04
ORD IDord-f7fd05ecc50b484fa0f4180bef3787f2
Source noteuspto-grants-2006_04