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HRID 279820作成日:2026年10月27日

Water → t-Butoxycarbonylglycyl thyroxine methyl ester

https://huagongshe.com/reaction/279820

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Ethyl AcetateHCID 8857—
反応物N-(tert-Butyloxycarbonyl)glycine N-hydroxysuccinimide esterHCID 76926—
反応物Methyl O-(4-hydroxy-3,5-diiodophenyl)-3,5-diiodo-L-tyrosinateHCID 13911218—
溶媒AcetoneHCID 180—
溶媒MethanolHCID 887—
生成物t-Butoxycarbonylglycyl thyroxine methyl esterHCID 18602701—

反応手順

To the aforesaid Boc-Gly-OSu solution the thyroxine methyl ester solution was added while ice cooling. After permitting the same to warm to room temperature, the mixture was stirred for 1.5 hr. After letting the reaction mixture stand overnight, 25 ml. of distilled water and 50 ml. of ethyl acetate were added thereto and the mixture was extracted with ethyl acetate. The extraction was repeated three times using 25 ml. of ethyl acetate. The ethyl acetate layers were combined and dried over anhydrous magnesium sulfate. The liquid was concentrated using a rotary evaporator and subjected to gel chromatography using a column filled with Sephadex LH-20 (made by Pharmacia Co., Ltd.). As the solvent, a mixture obtained by mixing acetone and methanol in a proportion of 4:1 (volume) was used. While confirming by TLC, the objective fraction was taken and concentrated under reduced pressure followed by crystallization. The product was obtained in an amount of 950 mg. (yield 82.5%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04587102
出典データセットuspto-grants-1986_05
ORD IDord-7ec2364d73ff4c30b447b924255c2d63
出典メモuspto-grants-1986_05