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HRID 1354062作成日:2026年10月27日

Water → 4-[4-(2,3-Dichlorophenyl)piperazin-1-yl]-1-(2, 3-dihydro-1H-indol-1-yl)butan-1-one

https://huagongshe.com/reaction/1354062

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DiisopropylethylamineHCID 81531—
反応物4-Chloro-1-(2,3-dihydro-1H-indol-1-yl)butan-1-oneHCID 3598062—
反応物1-(2,3-Dichlorophenyl)piperazine hydrochlorideHCID 11630372—
溶媒DimethylformamideHCID 6228—
生成物4-[4-(2,3-Dichlorophenyl)piperazin-1-yl]-1-(2, 3-dihydro-1H-indol-1-yl)butan-1-oneHCID 11952785113.5%

反応条件

温度45 °C

反応手順

A mixture of 1-(2,3-dichlorophenyl)piperazine, hydrochloride (8.0 g) and diisopropylethylamine (10 mL) in dimethyl formamide (50 mL) was heated to 45° C. followed by the addition of 4-chloro-1-(2,3-dihydro-1H-indol-1-yl)butan-1-one (6.7 g). The resulting mixture was heated at 100° C. for 6 h, cooled to room temperature and poured into water. The aqueous phase was extracted with diethyl ether, and the combined organic phases were dried (MgSO4), filtered and evaporated in vacuo to give a black oil (14.2 g). The oil was crystallised from acetone, and the formed crystals were recrystallised from ethanol to give a white crystalline material (3.8 g). Mp 134–136° C. 1H NMR (CDCl3): 1.90–2.05 (m, 2H); 2.45–2.60 (m, 4H); 2.65 (s, 4H); 3.00 (s, 4H); 3.20 (t, 2H); 4.10 (t, 2H); 6.90 (d, 1H); 7.00 (t, 1H); 7.05–7–25 (m, 4H); 8.25 (d, 1H). MS m/z: 418 (MH+), 299, 228, 188.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07223765B2
出典データセットuspto-grants-2007_05
ORD IDord-2148663ae566470eac44bfb98dfff919
出典メモuspto-grants-2007_05