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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 871866Generated: October 31, 2026

1-Cyclopropylpiperazine → HCID 67325292, compound

https://huagongshe.com/reaction/871866

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-CyclopropylpiperazineHCID 4742004—
Reactant2-(Difluoromethoxy)-4-fluoro-1-nitrobenzeneHCID 46311588—
SolventAcetonitrileHCID 6342—
ProductHCID 67325292HCID 6732529274.5%

Reaction Conditions

Temperature100 °C

Reaction Steps

To 2.07 g (10.0 mmol) of the product prepared in step 14.1 in 30 mL of acetonitrile are added 5.99 mL (35.0 mmol) of diispropylethylamine and then 2.09 g (10.5 mmol) of finely ground N-cyclopropylpiperazine (supplier). The reaction mixture is heated at 100°C. for 1 hour 30 minutes, cooled and concentrated under vacuum. The residue is taken up in 75 mL of ethyl acetate and washed with saturated aqueous NaHCO3 solution and with saturated aqueous NaCl solution. The organic phase is dried over Na2SO4, filtered and concentrated under vacuum. After triturating in cyclohexane, the solid is drained by suction and dried in an oven under vacuum. 2.33 g of the expected product are obtained in the form of a yellow solid, which is used as obtained in the following step. Yield=74.5%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08975250B2
Source datasetuspto-grants-2015_03
ORD IDord-18c0cf8960cc40a48365fed5a5882b76
Source noteuspto-grants-2015_03