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HRID 660754作成日:2026年10月24日

Triethylamine → (E)-4-[3-Benzyloxy-4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)-phenyl]-2-methyl-but-3-enenitrile

https://huagongshe.com/ja/reaction/660754

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物2-Methyl-3-butenenitrileHCID 27909—
反応物5-(2-Benzyloxy-4-iodophenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-oneHCID 68838643—
触媒palladium(II) acetateHCID 167845—
溶媒TetrahydrofuranHCID 8028—
生成物(E)-4-[3-Benzyloxy-4-(1,1,4-trioxo-1,2,5-thiadiazolidin-2-yl)-phenyl]-2-methyl-but-3-enenitrileHCID 68839915—

反応条件

温度110 °C

反応手順

A mixture of 2-methyl-but-3-enenitrile (18 mg, 0.225 mmol), 5-(2-benzyloxy-4-iodophenyl)-1,1-dioxo-1,2,5-thiadiazolidin-3-one (50 mg, 0.113 mmol), Pd(OAc)2 (5 mg, 0.023 mmol) and triethylamine (11 mg, 0.107 mmol) in THF (3 mL) is placed in a microwave vial and heated at 110° C. for 10 min. The mixture is filtered and the filtrate concentrated. The residue is purified by reverse phase HPLC to give the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08084448B2
出典データセットuspto-grants-2011_12
ORD IDord-14f89c40c83145309f7346db4efbc780
出典メモuspto-grants-2011_12