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HRID 406948作成日:2026年10月25日

Ethanesulfonic acid → (2R,4aR,10bR)-6-(2,6-Dimethoxy-pyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a, 10b-hexahydro-phenanthridin-2-ol ethansulfonate

https://huagongshe.com/reaction/406948

反応式

関与物質

役割名称HCID仕込み量
反応物Ethanesulfonic acidHCID 11668—
反応物(2R,4aR,10bR)-6-(2,6-Dimethoxy-pyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a,10b-hexahydro-phenanthridin-2-olHCID 11258441—
溶媒Methyl Isobutyl KetoneHCID 7909—
生成物(2R,4aR,10bR)-6-(2,6-Dimethoxy-pyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a, 10b-hexahydro-phenanthridin-2-ol ethansulfonateHCID 9104470996.9%

反応条件

温度50 °C

反応手順

(2R,4aR,10bR)-6-(2,6-Dimethoxy-pyridin-3-yl)-9-ethoxy-8-methoxy-1,2,3,4,4a,10b-hexahydro-phenanthridin-2-ol (1.5 g; 3.64 mmol) is dissolved in 9 ml of 4-methyl-2-pentanone. The solution is heated up to 50° C. 312 μl (3.82 mmol) of ethansulfonic acid are added. After crystallisation 3 ml 4-methyl-2-pentanon is added and the suspension is stirred over night. The crystals are filtered off and dried to obtain 1.78 g (94%) of the title compound (m.p.: 216° C.).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08754218B2
出典データセットuspto-grants-2014_06
ORD IDord-dfe6c45a927140359b23c19ce7a76efd
出典メモuspto-grants-2014_06