참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Iodide | HCID 4875 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Ammonium Hydroxide | HCID 14923 | — |
| 반응물 | Ammonium Acetate | HCID 517165 | — |
| 반응물 | 3-(3-Chloropropyl)-2-fluoro-4-iodopyridine | HCID 23657233 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 5-Iodo-1,2,3,4-tetrahydro-1,8-naphthyridine | HCID 57756253 | 69% |
반응 단계
A mixture of 3-(3-chloropropyl)-2-fluoro-4-iodopyridine (5.0 g, 17 mmol), NH4OH (100 mL, 800 mmol), ammonium acetate (18 g, 230 mmol), potassium iodide (5.5 g, 33 mmol), potassium carbonate (12 g, 87 mmol) and DMF (26 mL) was heated at 60° C. for 8 h. The mixture allowed to cool, and diluted with EtOAc. The layers were separated and the organic layer was washed with brine, dried with MgSO4, then concentrated under reduced pressure. The residue was purified by column chromatography on silica gel using CombiFlash® apparatus, eluting with 0 to 50% EtOAc in hexanes, to give the sub-title compound (3.0 g, 69% yield). LCMS calc. for C8H10IN2(M+H)+: m/z=261.0. Found: 261.1.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09200004B2 |
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| 출처 데이터셋 | uspto-grants-2015_12 |
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| ORD ID | ord-78e87c30a9734fc689d5da3dea89c409 |
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| 출처 메모 | uspto-grants-2015_12 |
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