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HRID 396192作成日:2026年10月24日

4-Chlorobutanal → HCID 10204932、化合物

https://huagongshe.com/ja/reaction/396192

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobutanalHCID 242200—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium borohydrideHCID 4311764—
反応物HCID 10177215HCID 10177215—
溶媒DimethylformamideHCID 6228—
溶媒Trifluoroacetic acidHCID 6422—
溶媒TetrahydrofuranHCID 8028—
生成物HCID 10204932HCID 1020493253%

反応手順

An amount of 100 mg (0.27 mmol) of 9-(2,4-dichloroanilino)-3,4-dihydro-2H-[1,4]oxazino[2,3-g]quinoline-8-carbonitrile, was stirred in N,N-dimethylformamide (2 mL), and to this was added a solution of 4-chloro-butyraldehyde (719 mg, 6.8 mmol) in tetrahydrofuran (2 mL) and trifluoroacetic acid (1.4 mL). The reaction mixture was stirred at room temperature, and to this was added sodium borohydride (128 mg, 3.4 mmol) portionwise, in 1.5 hours. The mixture was stirred for 16 hours, basified with saturated sodium bicarbonate solution, and extracted with ethyl acetate. After separation of the layers, the organic layer was washed with saturated brine solution, dried over sodium sulfate and evaporated to an oil. Purification was done by flash chromatography (10% acetone in dichloromethane) to give a yellow solid (66 mg, 53% yield), m.p 56-57° C.; 1H NMR (DMSO-d6) δ 9.92 (bs, 1H), 8.59 (s, 1H), 7.81 (d, 2H), 7.51 (m, 2H), 6.98 (s, 1H), 4.30 (t, 2H), 3.70 (t, 2H), 3.57 (t, 2H), 3.51 (t, 2H), 1.80 (m, 4H); HRMS (EI) m/z 461.06917 (M+1). Analysis for C22H19Cl3N4O.0.7CH3CO2C2H5.3.9H2O Found: C, 49.81; H, 3.78; N, 9.65. Calcd: C, 50.12; H, 5.46; N, 9.43.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06608048B2
出典データセットuspto-grants-2003_08
ORD IDord-cab0ee58e18c45aa9816c73f9f62eff8
出典メモuspto-grants-2003_08