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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 419744Generated: October 30, 2026

Isopropanol → HCID 178434473, compound

https://huagongshe.com/reaction/419744

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantHydrazine hydrate (1:1)HCID 24654—
Reactant1-(4,6-Dichloro-5-pyrimidinyl)ethanoneHCID 12278259—
Reactant4-[4-(4-fluoro-3-trifluoromethyl-phenyl)-1-methyl-1H-imidazol-2-yl]-piperidine dihydrochloride saltHCID 86632020—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
ProductHCID 178434473HCID 17843447350.29%

Reaction Conditions

Temperature0 °C

Reaction Steps

In a microwave vial charge 4-[4-(4-fluoro-3-trifluoromethyl-phenyl)-1-methyl-1H-imidazol-2-yl]-piperidine dihydrochloride salt (0.5 g, 1.0 eq), 1-(4,6-dichloro-pyrimidin-5-yl)-ethanone (0.22 g, 1.0 eq), TEA (1.2 mL, 8.0 eq) and isopropyl alcohol (5 mL). Stirr the reaction mass at 80° C. for 45 min in microwave. Monitor the reaction by TLC (10% MeOH in DCM). Cool the reaction mass to 0° C. and add hydrazine hydrate (0.07 mL, 1.2 eq). Slowly bring the reaction mass to RT. Stirr the reaction mass at 80° C. for 45 min in microwave. Monitor the reaction by TLC (10% MeOH in DCM). Concentrate the reaction mass under vacuum. Charge ethyl acetate and then wash with water and saturated aq. sodium chloride. Dry the organic layer over anhydrous Na2SO4 and concentrate it under reduced pressure. Purify the compound by column chromatography (Silica gel 60-120 mesh, DCM-Methanol). Crystallize the product in diethyl ether and filter it to give 4-(4-(4-(4-fluoro-3-(trifluoromethyl)phenyl)-1-methyl-1H-imidazol-2-yl)piperidin-1-yl)-3-methyl-1H-pyrazolo[3,4-d]pyrimidine (0.254 g, 50.29%). MS (M+H): m/z=460.5

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08093383B2
Source datasetuspto-grants-2012_01
ORD IDord-9606017a26c5431b848a9f680287c126
Source noteuspto-grants-2012_01