HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357583Generated: October 31, 2026
Potassium Carbonate → N-cyclopropyl-4-methyl-3-(1-(3-oxopiperazin-1-yl)phthalazin-6-yl)benzamide
https://huagongshe.com/reaction/2357583
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide | HCID 21914577 | — |
| Reactant | 4-(6-Bromophthalazin-1-yl)piperazin-2-one | HCID 68455278 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Dimethoxyethane ethanol | HCID 20074477 | — |
| Product | N-cyclopropyl-4-methyl-3-(1-(3-oxopiperazin-1-yl)phthalazin-6-yl)benzamide | HCID 11848245 | 84% |
Reaction Steps
A mixture of 4-(6-bromophthalazin-1-yl)piperazin-2-one (0.10 g, 326 μmol), N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (98mg, 326 μmol), and tetrakis(triphenylphosphine)palladium (19 mg, 16 μmol) in 5 mL DME/EtOH (4:1) was treated with 2M potassium carbonate (488 μl, 977 μmol). The resulting mixture was warmed up to 90° C. and stirred for 1 h under nitrogen. The mixture was cooled to room temperature, and the crude product was purified via flash chromatography (silica gel) eluting with a gradient of 4% 2 M ammonia in MeOH/DCM to 6% 2 M ammonia in MeOH/DCM to give the title compound (0.11 g) as a pale yellow solid. Found MS(ES+): 402(M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07759337B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-3e39f7ebe9c44c18835196d9e8bb646f |
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| Source note | uspto-grants-2010_07 |
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