Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2357561생성일: 2026년 10월 27일
Potassium Carbonate → N-cyclopropyl-3-(1-(2,4-dimethylphenyl)phthalazin-6-yl)-4-methylbenzamide
https://huagongshe.com/reaction/2357561
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 2-(Dicyclohexylphosphino)-2'-methylbiphenyl | HCID 2734938 | — |
| 반응물 | N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide | HCID 21914577 | — |
| 반응물 | 6-chloro-1-(2,4-dimethylphenyl)Phthalazine | HCID 68454866 | — |
| 촉매 | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| 용매 | Methanol | HCID 887 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | N-cyclopropyl-3-(1-(2,4-dimethylphenyl)phthalazin-6-yl)-4-methylbenzamide | HCID 68452425 | — |
반응 단계
A mixture of 6-chloro-1-(2,4-dimethylphenyl)phthalazine (150 mg, 558 μmol), N-cyclopropyl-4-methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzamide (437 mg, 1450 μmol), 2-(dicyclohexylphosphino)-2′-methylbiphenyl (18.3 mg, 50.2 μmol, Strem), Pd2(dba)3 (15.3 mg, 16.7 μmol, Strem), and potassium carbonate (231 mg, 1674 μmol) in Dioxane:H2O=4:1 (5 mL) was heated to 80° C. for 18 h. After cooling to room temperature, the mixture was diluted with MeOH and concentrated over SiO2. The residue was purified with column chromatography (MeOH/CH2Cl2=0-4%). The residue was purified with reverse-phase chromatography (Phenomenex Synergi 4m Max RP 80 A column, 150×21 mm, 20 mL/min, 10-95% CH3CN/H2O, 0.1% TFA, 10.5 min gradient). Yield: 113 mg (50%). MS (ESI, pos. ion) m/z: 408 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07759337B2 |
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| 출처 데이터셋 | uspto-grants-2010_07 |
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| ORD ID | ord-0a582763ec8c4a5d9a829294ca033bc5 |
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| 출처 메모 | uspto-grants-2010_07 |
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