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HRID 729291作成日:2026年10月27日

3-Chloro-4-morpholinoaniline → 2-Butyl-4-[(3-chloro-4-morpholin-4-ylphenyl)amino]-5-phenylisothiazol-3(2H)-one 1,1-dioxide

https://huagongshe.com/reaction/729291

反応式

関与物質

役割名称HCID仕込み量
反応物3-Chloro-4-morpholinoanilineHCID 108661—
反応物2-Butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 67242623—
溶媒AcetonitrileHCID 6342—
生成物2-Butyl-4-[(3-chloro-4-morpholin-4-ylphenyl)amino]-5-phenylisothiazol-3(2H)-one 1,1-dioxideHCID 117198599%

反応手順

A solution of 2-butyl-4-chloro-5-phenylisothiazol-3(2H)-one 1,1-dioxide (0.025 g, 0.083 mmol) and 3-chloro-4-morpholinoaniline (0.039 g, 0.183 mmol) in MeCN (1 ml) was heated in a microwave reactor at 130° C. for 90 mins. The product was purified by preparative HPLC (Kromasil C8, 0.1M NH4OAc/MeCN, gradient). The combined product fractions were evaporated and freeze-dried to give the title compound (0.004 mg, 9%). 1H NMR (400 MHz, CD3CN): δ 7.74 (bs, 1H), 7.29-7.24 (m, 1H), 7.20-7.15 (m, 2H), 7.12-7.08 (m, 2H), 6.80-6.75 (m, 3H), 3.76-3.71 (m, 6H), 2.85-2.81 (m, 4H), 1.85-1.76 (m, 2H), 1.52-1.42 (m, 2H), 1.00 (t, 3H); Mass Spectrum: M+H+ 476.

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-951f80639f3f4bdc941c46291d947b7d
出典メモuspto-grants-2009_09