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HRID 1051883作成日:2026年10月27日

Toluene → (cis) (4-(4-Chloroindolin-1-yl)thiazol-2-yl) (2,6-dimethylmorpholino) methanone

https://huagongshe.com/reaction/1051883

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物4-ChloroindolineHCID 3016306—
反応物Sodium t-butoxideHCID 23676156—
反応物(cis) (4-Bromothiazol-2-yl) (2,6-dimethylmorpholino)methanoneHCID 118444688—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Ethyl AcetateHCID 8857—
生成物(cis) (4-(4-Chloroindolin-1-yl)thiazol-2-yl) (2,6-dimethylmorpholino) methanoneHCID 11844468560.6%

反応条件

温度100 °C

反応手順

(cis) (4-bromothiazol-2-yl) (2,6-dimethylmorpholino)methanone (step-1 of compound 45, 1.0 g, 3.28 mmol) and 4-chloroindoline (0.55 g, 3.60 mmol) were added to seal tube containing toluene (25 ml). Sodium tert-butoxide (0.47 g. 4.91 mmol) was added, the nitrogen gas was bubbled through reaction mixture for 15 minutes and tris(dibenzylideneacetone)dipalladium(0) (0.15 g, 0.16 mmol) was added under nitrogen and the tube was sealed. The reaction mixture was heated at 100° C. for 18 hr under stirring. The progress of reaction was monitored by TLC. The reaction mixture was cooled to 25° C. and diluted with ethyl acetate (100 ml) and washed with water (25 ml). The organic layer was dried over sodium sulfate filtered and concentrated under reduced pressure to obtain a crude product; which was purified by flash column chromatography using 15% ethyl acetate in hexanes as an eluent to obtain the title compound (0.75 g, 60.6%). MS: m/z 378 (M+1).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09388196B2
出典データセットuspto-grants-2016_07
ORD IDord-3261e83e92d849728003b467ffd60899
出典メモuspto-grants-2016_07