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HRID 352356作成日:2026年10月26日

Cesium carbonate → cis-1-Acetyl-5-methoxy-6-(3,4,5-trimethylpiperazin-1-yl)indoline

https://huagongshe.com/reaction/352356

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Binap, (A+-)-HCID 634876—
反応物1-Acetyl-6-bromo-5-methoxyindolineHCID 21948375—
反応物(2R,6S)-1,2,6-TrimethylpiperazineHCID 30720221—
触媒palladium(II) acetateHCID 167845—
生成物cis-1-Acetyl-5-methoxy-6-(3,4,5-trimethylpiperazin-1-yl)indolineHCID 6966392423%

反応手順

A mixture of palladium (II) acetate (500 mg), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (2.0 g) and cesium carbonate (10.3 g) in dry degassed 1,4-dioxane (120 ml) under argon was sonicated at 28° C. for 0.5 h producing a pink heterogeneous mixture. This was treated with D1 (6.0 g, 22 mmole) followed by cis-1,2,6-trimethylpiperazine (J. Med. Chem. 1968, 11, 592; 4.8 g, 38 mmole) and heated with rapid stirring at reflux for 70 h. The mixture was allowed to cool, filtered, then concentrated under vacuum. The residue was treated with water and extracted with EtOAc. The organic solution was then extracted with 1M HCl acid and the aqueous extract was basified by addition of K2CO3 and extracted with EtOAc. The extract was dried (Na2SO4) and concentrated under vacuum to leave an orange solid, which was chromatographed on silica gel eluting with 0-10% MeOH/DCM to afford the required product as a pale yellow solid (1.6 g, 23%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06747030B1
出典データセットuspto-grants-2004_06
ORD IDord-0e200c4f699442a2bd2ffad183f4181a
出典メモuspto-grants-2004_06