参与物
| 角色 | 名称 | HCID | 投料 |
|---|
| 反应物 | POTASSIUM DIPHOSPHATE | HCID 62657 | — |
| 反应物 | 2-碘苯甲酸甲酯 | HCID 69132 | — |
| 反应物 | 2-双环己基膦-2',6'-二甲氧基联苯 | HCID 11269872 | — |
| 反应物 | 3-甲基异恶唑-5-甲胺 | HCID 16481072 | — |
| 催化剂 | 三(二亚苄基丙酮)二钯 | HCID 9811564 | — |
| 溶剂 | 聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯] | HCID 962 | — |
| 溶剂 | 甲苯 | HCID 1140 | — |
| 产物 | Methyl 2-{[(3-methylisoxazol-5-yl)methyl]amino}-benzoate | HCID 57440405 | 45.6% |
反应步骤
1-(3-Methylisoxazol-5-yl)methanamine (155 mg, 1.37 mmol, 1.2 eq), potassium phosphate (341 mg, 1.60 mmol, 1.4 eq), S-Phos (95 mg, 0.230 mmol, 0.2 eq) and Pd2dba3 (13 mg, 0.06 mmol, 0.05 eq) were stirred in toluene (5 ml) under nitrogen. Methyl 2-iodobenzoate (300 mg, 1.14 mmol, 1 eq) was added and the mixture was stirred at room temperature for 3 days, then at 90° C. for 6 h. The reaction mixture was allowed to cool, poured into water (100 ml) and extracted with ethyl acetate (3×60 ml). The combined extracts were washed with brine, dried over MgSO4, filtered and evaporated. The residual gummy oil was triturated with ether resulting in precipitation of a small amount of a yellow solid which was filtered off. The filtrate was evaporated and triturated again with methanol and a second precipitate was removed by filtration. The filtrate was evaporated, then purified by silica column chromatography, eluting with DCM. The product fractions were evaporated to afford methyl 2-{[(3-methylisoxazol-5-yl)methyl]amino}-benzoate as a yellow oily gum (128 mg, 45% yield); 1H NMR (399.902 MHz, CDCl3) δ 2.25 (s, 3H), 3.88 (s, 3H), 4.53 (d, 2H), 5.99 (s, 1H), 6.62-6.70 (m, 2H), 7.32-7.38 (m, 1H), 7.92-7.96 (m, 1H), 8.19 (t, 1H). MS: m/z 247 (MH+)
来源与证据
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 专利号 | US07737149B2 |
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| 来源数据集 | uspto-grants-2010_06 |
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| ORD ID | ord-2140c456723b4dd89e67c4192e737bb4 |
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| 来源说明 | uspto-grants-2010_06 |
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