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HRID 273989作成日:2026年10月26日

Pyridine → 7-[[(1,1-Dimethylethyl)dimethylsily]oxy]-1,2,3,4-tetrahydro-6-methoxyisoquinoline

https://huagongshe.com/reaction/273989

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物tert-Butyldimethylsilyl chlorideHCID 28928—
反応物7-Methoxy-1,2,3,4-tetrahydroisoquinolin-6-olHCID 417289—
生成物7-[[(1,1-Dimethylethyl)dimethylsily]oxy]-1,2,3,4-tetrahydro-6-methoxyisoquinolineHCID 15285554—

反応手順

To a solution of 19.2 g of 6-hydroxy-7-methoxy-1,2,3,4-tetrahydroisoquinoline in 425 mL of pyridine is added 48.4 g of t-butyl-dimethylsilylchloride and 0.5 g of 4-N,N-dimethylaminopyridine. The solution is heated to reflux for 3.5 hours and the volatiles removed at 70° C. by distillation. The residue is partitioned between aqueous potassium bicarbonate and ethyl acetate. The organic layer is washed with water, dried (magnesium sulfate) and the volatiles removed in vacuo. The residue is suspended in diethyl ether, filtered and washed with hexane. The filtrate is evaporated and the residue distilled via Kugelrohr at 150 mm and 120°-130° C. to afford 26.2 g of the desired product as a colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387685
出典データセットuspto-grants-1995_02
ORD IDord-0884c459a87e475f9bd46a231412b209
出典メモuspto-grants-1995_02