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HRID 414869作成日:2026年10月25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/414869

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-l,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 NRR spectrum which was consistent with structure 21.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04794191
出典データセットuspto-grants-1988_12
ORD IDord-df871e310d6c4343b1253da7c7c8b2b6
出典メモuspto-grants-1988_12