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HRID 333981作成日:2026年10月27日

Cesium carbonate → tert-Butyl 3-(2-methoxy-2-oxo-ethyl)-4-(2-methyl-4-quinolyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/333981

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物4-Chloro-2-methylquinolineHCID 77973—
反応物1,1'-(9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(1,1-diphenylphosphine)HCID 636044—
反応物Methyl 4-Boc-piperazine-2-acetateHCID 2756816—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒TolueneHCID 1140—
生成物tert-Butyl 3-(2-methoxy-2-oxo-ethyl)-4-(2-methyl-4-quinolyl)piperazine-1-carboxylateHCID 8669160117.4%

反応条件

温度110 °C

反応手順

4-Chloroquinaldine (263 mg, 1.481 mmol), tert-butyl 3-(2-methoxy-2-oxo-ethyl)piperazine-1-carboxylate (318 mg, 1.231 mmol) and caesium carbonate (885 mg, 2.72 mmol) were mixed with anhydrous toluene (4 ml) in an argon atmosphere. 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (128 mg, 0.221 mmol) and tris(dibenzylideneacetone)dipalladium(0) (67 mg, 0.073 mmol) were added and the resulting mixture was stirred at 110° C. for six hours. Additional 9,9-dimethyl-4,5-bis(diphenylphosphino)xanthene (128 mg, 0.221 mmol) and tris(dibenzylideneacetone)dipalladium(0) (67 mg, 0.073 mmol) were added and the mixture was stirred at 110° C. overnight. After reaching room temperature the mixture was filtered, the filtrate was evaporated to dryness to give a red oil that was purified by column chromatography (silica, gradient from DCM to DCM/methanol 1:20) to yield 136 mg of a yellow foam (0.214 mmol, 17%). MS (ESI) m/z=400.2 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08883791B2
出典データセットuspto-grants-2014_11
ORD IDord-80add02432bd4de7aa17912980a74a87
出典メモuspto-grants-2014_11