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HRID 551965作成日:2026年10月26日

Acetic Acid → Methyl 5-{butyl[4-(phenylethynyl)benzyl]amino}-2-fluorobenzoate

https://huagongshe.com/reaction/551965

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物ButanalHCID 261—
反応物4-(Phenylethynyl)benzaldehydeHCID 609908—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物Methyl 5-amino-2-fluorobenzoateHCID 15621043—
溶媒WaterHCID 962—
溶媒TolueneHCID 1140—
生成物Methyl 5-{butyl[4-(phenylethynyl)benzyl]amino}-2-fluorobenzoateHCID 5755448375.1%

反応条件

温度70 °C

反応手順

A solution of methyl 5-amino-2-fluorobenzoate (500 mg, 2.96 mmol), 4-(phenylethynyl)benzaldehyde (6 10 mg, 2.96 mmol) and acetic acid (0.25 mL, 4.40 mmol) in toluene (20 mL) was heated under reflux for 3 h with azeotropic removal of water. Then the solvent was removed by distillation at atmospheric pressure and replaced by anhydrous DCE (20 mL). Butanal (Fluka, 0.66 mL, 7.39 mmol), sodium triacetoxyborohydride (1880 mg, 8.87 mmol) and acetic acid (0.25 mL, 4.40 mmol) were added and the resulting mixture was heated at 70° C. After 45 min, an additional amount of sodium triacetoxyborohydride (630 mg, 2.96 mmol) was added. After 45 min, the reaction mixture was diluted with water (40 mL) and extracted with DCM (3×20 mL). The combined organic layers were dried over MgSO4 and the solvents were removed under reduced pressure. Purification by flash chromatography on silicagel (cHex/EtOAc): gave. 924 mg (75%) of the title compound as a colorless oil. HPLC, Rt: 5.6 min (purity: 99.8%). LC/MS, M+(ESI): 416.1. 1H NMR (CDCl3) δ: 7.51-7.44 (m, 4H), 7.32 (m, 3H), 7.17 (m, 3H), 6.92 (dd, J=9.8, 9.7 Hz, 1H), 6.73 (m, 1H), 4.49 (s, 2H), 3.88 (s, 3H), 3.36 (t, J=7.2 Hz, 2H), 1.60 (m, 2H), 1.34 (m, 2H), 0.93 (t, J=7.2 Hz, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947851B2
出典データセットuspto-grants-2011_05
ORD IDord-1070f5b0b7db4b6598ffb3e68c69fe06
出典メモuspto-grants-2011_05