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HRID 15820作成日:2026年10月26日

Cesium carbonate → Tert-butyl 4-(2-methylquinolin-5-yl)piperazine-1-carboxylate

https://huagongshe.com/reaction/15820

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tert-Butyl piperazine-1-carboxylateHCID 143452—
反応物Bis(diphenylphosphino)-1,1'-binaphthylHCID 18630801—
反応物2-Methylquinolin-5-yl trifluoromethanesulfonateHCID 49851899—
触媒palladium(II) acetateHCID 167845—
溶媒TolueneHCID 1140—
生成物Tert-butyl 4-(2-methylquinolin-5-yl)piperazine-1-carboxylateHCID 49851900—

反応条件

温度95 °C

反応手順

A solution of 2-methyl-5-quinolinyl trifluoromethanesulfonate (lwt, 1 eq) in toluene (7 vol) was degassed under reduced pressure then flushed with nitrogen. To the mixture were added N-Boc-piperazine (1.05 eq), milled cesium carbonate (1.5 eq), (+/−)-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP, 0.15 eq) and palladium acetate (0.05 eq). The resulting mixture was stirred at 95° C. for 16 hours. The solution was cooled and concentrated to approx. 4 vol and 10 vol of cyclohexane were added giving a suspension. The suspension was stirred for 30 minutes and filtered over a pad of Silica Gel (approx 2.5 vol). The filtrate was washed with 10 vol of water and concentrated under reduced pressure to give the title compound as a brown solid, which was carried through directly to the next stage.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07732600B2
出典データセットuspto-grants-2010_06
ORD IDord-139e0c730c15469ca499aa8643504939
出典メモuspto-grants-2010_06