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HRID 2292322作成日:2026年10月27日

Thyroxine → 4-Acetoxy-3,5-bis[N,N-bis(t-butoxycarbonylmethyl)aminomethyl]-3'-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-beta-methoxycarbonylphenethyl]benzophenone

https://huagongshe.com/reaction/2292322

反応式

関与物質

役割名称HCID仕込み量
反応物ThyroxineHCID 5819—
反応物TetrahydrofuranHCID 8028—
反応物2-Ethoxy-1-(ethoxycarbonyl)-1,2-dihydroquinolineHCID 27833—
反応物4-Acetoxy-3,5-bis[N,N-bis(t-butoxycarbonylmethyl)aminomethyl]-3'-carboxybenzophenoneHCID 14405513—
生成物4-Acetoxy-3,5-bis[N,N-bis(t-butoxycarbonylmethyl)aminomethyl]-3'-[4-(4-hydroxy-3,5-diiodophenoxy)-3,5-diiodo-beta-methoxycarbonylphenethyl]benzophenoneHCID 86741575—

反応手順

A mixture of 900 mg of 20 and 0.265 g (1.07 mmol) of 1-carbethoxy-2-ethoxy-1,2-dihydroquinoline (EEDQ) in 20 mL of dry tetrahydrofuran was stirred for 30 minutes and 0.85 g (1.07 mmol) of the methyl ester of thyroxine was added. The mixture was stirred overnight. The reaction mixture was purified by gel permeation chromatography using tetrahydrofuran as the solvent, giving 630 mg of material which showed an NMR spectrum which was consistent with structure 21.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04801722
出典データセットuspto-grants-1989_01
ORD IDord-7454a9445f7f41348a67ce5c19ea6fd0
出典メモuspto-grants-1989_01