참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Iodo-o-toluidine | HCID 83221 | — |
| 반응물 | 3-Fluoropyridine-4-carboxylic acid | HCID 345361 | — |
| 반응물 | Lithium Hexamethyldisilazide | HCID 2733832 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 3-[(2-Methyl-4-iodophenyl)amino]isonicotinic acid | HCID 57649617 | 59% |
반응 단계
4-Iodo-2-methylaniline (233 mg, 1.00 mmol) and 3-fluoropyridine-4-carboxylic acid (141 mg, 1.00 mmol) were dissolved in dry THF (6.0 ml) under argon and the mixture was cooled to −78° C. A solution of LiHMDS (1.0M in THF, 3.5 ml) was added and the reaction mixture was allowed to warm to ambient temperature. After 36 h the reaction was quenched by adding solid NH4Cl. After filtration the volatiles were removed in vacuo and the crude material was purified by flash chromatography using silica gel and a gradient of 0-10% methanol in DCM as eluent to give 208 mg (588 μmol; 59% yield) of pure desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08198457B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-4dcdc5fccc404de8bfc41e4c2c342018 |
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| 출처 메모 | uspto-grants-2012_06 |
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