참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Nitrogen | HCID 947 | — |
| 반응물 | Potassium Phosphate, Tribasic | HCID 62657 | — |
| 반응물 | 4-Carboxy-3-fluorophenylboronic acid | HCID 2763201 | — |
| 반응물 | 6-Chloro-4-hydrazinyl-2-(4-phenoxyphenyl)nicotinonitrile | HCID 86665697 | — |
| 촉매 | HCID 178418807 | HCID 178418807 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | HCID 69670585 | HCID 69670585 | — |
반응 단계
A solution of 6-chloro-4-hydrazinyl-2-(4-phenoxyphenyl)nicotinonitrile (9.5 mg, 0.028 mmol), 4-borono-2-fluorobenzoic acid (14.5 mg, 0.079 mmol), 2 M aqueous potassium phosphate (0.071 mL, 0.141 mmol) and PdCl2(dppf)-CH2Cl2 adduct (4.6 mg, 5.63 μmol) in DMF (0.45 mL) was degassed by vacuum-N2 refill cycle twice. The sealed tube was then heated at 85° C. under N2. After 1.5 h, no desired product was detected. Additional 4-borono-2-fluorobenzoic acid (21.4 mg), PdCl2(dppf)-CH2Cl2 adduct (11 mg), potassium phosphate (0.14 mL) and DMF (0.3 mL) were added. The mixture was again degassed by vacuum-N2 refill cycle twice and stirred at 85° C. for 20 h. The mixture was diluted with 1 N aqueous HCl (0.7 mL) and MeOH (0.8 mL), and purified by reverse phase HPLC (Sunfire S10 30×250 mm column), eluting with 60-90% solvent B (10% methanol-90% water-0.1% TFA) in solvent A (90% methanol-10% water-0.1% TFA), to give Example 245 as yellow powder (2.7 mg, 14% yield), assumed as bis-TFA salt. 1H NMR (400 MHz, methanol-d4) δ ppm 8.15 (1H, t, J=7.65 Hz), 7.89-7.93 (2H, m), 7.86 (1H, s), 7.77-7.84 (2H, m), 7.44-7.50 (2H, m), 7.24-7.30 (3H, m), 7.15-7.19 (2H, m); MS (ES+) m/z: 441.2 (M+H); LC retention time: 3.438 min (analytical HPLC Method A).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08846673B2 |
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| 출처 데이터셋 | uspto-grants-2014_09 |
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| ORD ID | ord-81e8e847c17a4d47869d596b2c235dbf |
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| 출처 메모 | uspto-grants-2014_09 |
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