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HRID 729275作成日:2026年10月26日

1-(5-Amino-1-benzofuran-2-yl)ethanone → 4-[(2-Acetyl-1-benzofuran-5-yl)amino]-2-butyl-5-phenylisothiazol-3(2H)-one 1,1-dioxide

https://huagongshe.com/reaction/729275

反応式

関与物質

役割名称HCID仕込み量
反応物1-(5-Amino-1-benzofuran-2-yl)ethanoneHCID 3783367—
反応物2-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 67242623—
溶媒AcetonitrileHCID 6342—
生成物4-[(2-Acetyl-1-benzofuran-5-yl)amino]-2-butyl-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 1150304929,393,388%

反応条件

温度130 °C

反応手順

A mixture of 2-butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide (300 mg, 0.90 nmol) and 1-(5-amino-1-benzofuran-2-yl)ethanone (387 mg, 2.21 mmol) in dry MeCN (4.5 mL) was heated in a microwave reactor at 130° C. for 1 h, then at 130° C. for 1 h, then at 140° C. for 1 h and finally at 140° C. for 1.5 h. The mixture was purified using preparative HPLC (Kromasil-column C8, 0.1M NH4OAc/MeCN, gradient) to give the title compound (116 mg, 28%); 1H NMR (400 MHz, CD3CN): δ 7.86 (bs, 1H), 7.34-7.32 (m, 1H), 7.26-7.22 (m, 1H), 7.03-7.15 (m, 7H), 3.76 (t, 2H), 1.78-1.87 (m, 2H) 1.43-1.54 (m, 2H), 1.05 (t, 3H); Mass Spectrum: M−H+ 437

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07582629B2
出典データセットuspto-grants-2009_09
ORD IDord-f86d8678885b459999024205244d1183
出典メモuspto-grants-2009_09