참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Ammonium Chloride | HCID 25517 | — |
| 반응물 | 2-Chlorophenylboronic acid | HCID 2734322 | — |
| 반응물 | 5-Bromo-3-iodo-1-phenylpyridin-2(1H)-one | HCID 22318957 | — |
| 반응물 | 5-Bromo-3-(2-chlorophenyl)-1-phenyl-1,2-dihydropyridin-2-one | HCID 22319040 | — |
| 반응물 | HCID 178478990 | HCID 178478990 | — |
| 촉매 | HCID 178418745 | HCID 178418745 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-(2-Chlorophenyl)-5-cyclohexyl-1-phenyl-1,2-dihydropyridin-2-one | HCID 22319069 | — |
반응 단계
30 mg of 5-bromo-3-(2-chlorophenyl)-1-phenyl-1,2-dihydropyridin-2-one synthesized from 5-bromo-1-phenyl-3-iodo-1,2-dihydropyridin-2-one and 2-chlorophenyl boronic acid in accordance with the method of Referential Example 3 was dissolved in 20 ml of tetrahydrofuran, followed by adding 1 mg of [1,3-bis(diphenylphosphino)propane]nickel (II) chloride. Under stirring in nitrogen atmosphere, 0.1 ml of cyclohexyl magnesium chloride (2.0M ether solution) was added dropwise thereinto. After stirring at room temperature in nitrogen atmosphere overnight, the mixture was heated under reflux for 1 hour. After cooling to room temperature, a saturated aqueous solution of ammonium chloride was added thereto, followed by extracting with ethyl acetate. The organic layer was washed with brine and dried over anhydrous magnesium sulfate. The solvent was evaporated, and the residue was purified by silica gel chromatography (chloroform/methanol system), to give 6 mg of the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07939549B2 |
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| 출처 데이터셋 | uspto-grants-2011_05 |
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| ORD ID | ord-cfcde7b60ad24e15b48a7395372ec5b4 |
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| 출처 메모 | uspto-grants-2011_05 |
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