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HRID 77323作成日:2026年10月26日

Tetramethyltin → N-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl ester

https://huagongshe.com/reaction/77323

反応式

関与物質

役割名称HCID仕込み量
反応物TetramethyltinHCID 11661—
反応物Lithium ChlorideHCID 433294—
反応物N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 86653275—
触媒HCID 178479802HCID 178479802—
溶媒DimethylformamideHCID 6228—
生成物N-Isoamyl-N-(6-methyl naphthalene-2-sulfonyl)-D-valine tert-butyl esterHCID 6715528450%

反応条件

温度80 °C

反応手順

To a solution of N-isoamyl-N-(6-trifluoromethanesulfonyloxy naphthalene-2-sulfonyl)-D-valine tert-butyl ester (1.1 g, 1.89 mmol) in N,N-dimethylformamide (20 mL) is added lithium chloride (0.40 g, 9.5 mmol), tetramethyl tin (0.525 mL, 3.79 mmol), and bistriphenylphosphino palladium dichloride (0.066 g, 0.095 mmol). The reaction is heated to 80° C. for 16 h. The reaction is allowed to cool to ambient temperature and filtered through Celite. The filtrate is poured over water and extracted three times with dichloromethane. The combined organic extracts were washed with brine, dried over sodium sulfate, and concentrated in vacuo. The residue is purified by column chromatography (4% hexanes-ethyl acetate) to afford the title compound as a white solid (0.41 g, 50% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08841291B2
出典データセットuspto-grants-2014_09
ORD IDord-457daebb59124a8c80dea501b501c76d
出典メモuspto-grants-2014_09