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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1929412Generated: October 25, 2026

Phosphoric Acid → (3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]-methanone phosphate hydrate

https://huagongshe.com/reaction/1929412

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphoric AcidHCID 1004—
ReactantPruvanserinHCID 6433122—
SolventEthanolHCID 702—
Product(3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]-methanone phosphate hydrateHCID 68837267188.5%

Reaction Conditions

Temperature75 °C

Reaction Steps

Add (3-cyano-1H-indol-7-yl)-[4-(4-fluorophenethyl)piperazin-1-yl]methanone (300.0 g, 797 mmol.) and anhydrous ethanol (15 L, denatured with toluene) to a 22 L flask equipped with overhead agitation, heating mantle, and condenser. Heat the slurry to about 75° C. to provide a homogeneous solution. Add a solution of 1 M aqueous phosphoric acid (877 mL, 877 mmol, 1.1 equiv) over 10 minutes while maintaining the temperature above 72° C. The salt may begin precipitating after approximately 380 mL of phosphoric acid solution is added. Remove the heating mantle after the addition is complete, and allow the slurry to cool to about 22° C. Cool the slurry to about 5° C. and stir for about 2 hours. Filter the mixture and wash the cake three times with 500 mL cold ethanol. Dry the solid overnight in a vacuum oven at about 50° C. to provide 370 g (98% yield) of the title crystal form as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08188087B2
Source datasetuspto-grants-2012_05
ORD IDord-befc1f8f8d31425b8f0f88d33e5b5633
Source noteuspto-grants-2012_05