참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | 2-Bromo-5-methylthiophene | HCID 69831 | — |
| 반응물 | 5-Chloro-1,10-phenanthroline | HCID 77865 | — |
| 반응물 | 2,2-dimethyl-N-(5-methyl-1,3-thiazol-2-yl)propanamide | HCID 17190929 | — |
| 반응물 | Water ammonium hydroxide | HCID 86589665 | — |
| 용매 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 생성물 | HCID 178426236 | HCID 178426236 | — |
반응 단계
In a 4 mL vial charged with a stir bar, 2,2-dimethyl-N-(5-methyl-1,3-thiazol-2-yl)propanamide (62 mg, 0.3 mmol, Example 87A) was added, followed by copper(I) trifluoromethanesulfonate benzene complex (31 mg, 0.06 mmol), 5-chloro-1,10-phenanthroline (26 mg, 0.12 mmol) and cesium carbonate (107 mg, 0.33 mmol). A loose cap with septum was placed on the vial and then the vial was placed under vacuum in a vacuum oven for 30 minutes. The mixture was purged with nitrogen gas a couple of times. Then 2-bromo-5-methylthiophene (58 mg, 0.33 mmol) dissolved in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the solid mixture. The vial was capped and placed on a heater/stirrer and heated to 120° C. overnight. Then 1 mL of a solution of concentrated ammonium hydroxide/water (1:2) was added. The reaction was filtered and concentrated to dryness. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid) to provide the title compound.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08383657B2 |
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| 출처 데이터셋 | uspto-grants-2013_02 |
|---|
| ORD ID | ord-7e47200319224a43ab67caee20c0c6b9 |
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| 출처 메모 | uspto-grants-2013_02 |
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