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HRID 131356作成日:2026年10月27日

4,4,4-Trifluorobutanoic acid → N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazapin-3-yl)-4,4,4-trifluoro-butyramide

https://huagongshe.com/reaction/131356

反応式

関与物質

役割名称HCID仕込み量
反応物4,4,4-Trifluorobutanoic acidHCID 2777085—
反応物3-amino-1H-1,5-benzodiazepine-2,4(3H,5H)-dioneHCID 21955806—
触媒4-(Dimethylamino)pyridineHCID 14284—
溶媒DimethylformamideHCID 6228—
生成物N-(2,4-Dioxo-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazapin-3-yl)-4,4,4-trifluoro-butyramideHCID 5862604074%

反応手順

Combine 3-amino-1H-1,5-benzodiazepine-2,4-(3H, 5H)-dione (5.60 g, 29.3 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimde hydrochloride (6.75 g, 35.2 mmol) and 4(dimethylamino)pyridine (0.183 g, 1.5 mmol) in 100 mL DMF, add 4,4,4-trifluoro butyric acid dropwise at 0-5° C. After addition, stir the reaction mixture at ice-water. After half an hour, warm to RT. After stirring overnight, remove solvent DMF under reduce pressure and suspend the residue in 200 mL of mixed solvent (CHCl3: i-PrOH=3:1). Collect the solid via vacuum filtration to give the title compound (6.87 g, yield 74%): mass spectrum (APCI) (m/e): 316.1 (M+1); 1H NMR (400 MHz, DMSO-d6): δ 10.72 (s, 2H), 8.60 (d, 1H, J=7.2 Hz), 7.24-7.15 (m, 4H), 4.74 (d, 1H, J=7.2 Hz), 2.58 (t, 2H, J=7.2 Hz), 2.39-2.35 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07384934B2
出典データセットuspto-grants-2008_06
ORD IDord-de96973e6ca942bba5431d5ecdb42ab3
出典メモuspto-grants-2008_06