Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Isopropanol | HCID 3776 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 1-(4,6-Dichloro-5-pyrimidinyl)ethanone | HCID 12278259 | — |
| Reactant | 4-[4-(4-fluoro-3-trifluoromethyl-phenyl)-1-methyl-1H-imidazol-2-yl]-piperidine dihydrochloride salt | HCID 86632020 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 178434473 | HCID 178434473 | 50.29% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08093383B2 |
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| Source dataset | uspto-grants-2012_01 |
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| ORD ID | ord-9606017a26c5431b848a9f680287c126 |
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| Source note | uspto-grants-2012_01 |
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