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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241978Generated: October 30, 2026

Acetonitrile → HCID 12004312, compound

https://huagongshe.com/reaction/2241978

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantHCID 1530394HCID 1530394—
ProductHCID 12004312HCID 12004312—

Reaction Steps

1,2-benz-isoxazole-3-trifluoromethyl sulfonate I (Step 1, 0.50 g) and 4-(4-(2-methoxyphenyl)piperazin-1-yl)piperidine (Example G, Step 2, above, 0.514 g) were added to a cold suspension of CsCO3 (0.92 g) in acetonitrile (6 mL) under vigorous stirring. The reaction mixture was stirred at room temperature for 48 hours. The mixture was then filtered and concentrated on a rotary evaporator. The residue was dissolved in water extracted with CH2Cl2, dried over anhydrous MgSO4, filtered and concentrated on a rotary evaporator. The desired product was purified by flash chromatography on silica gel using ethyl acetate/hexane to give 0.34 g as an off-white solid; MP 71-73° C.; MS (ES) m/z (relative intensity): 393 (M+H)+ (100).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07671056B2
Source datasetuspto-grants-2010_03
ORD IDord-15aab7ab9ee24f56934a9bf89eeee401
Source noteuspto-grants-2010_03