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HRID 16769生成日期:2026年10月23日

POTASSIUM DIPHOSPHATE → Methyl 2-{[(3-methylisoxazol-5-yl)methyl]amino}-benzoate

https://huagongshe.com/zh-CN/reaction/16769

反应方程式

参与物

角色名称HCID投料
反应物POTASSIUM DIPHOSPHATEHCID 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}-benzoateHCID 5744040545.6%

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

DOI10.6084/m9.figshare.5104873.v1
专利号US07737149B2
来源数据集uspto-grants-2010_06
ORD IDord-2140c456723b4dd89e67c4192e737bb4
来源说明uspto-grants-2010_06