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HRID 265082作成日:2026年10月27日

N-Hydroxysuccinimide → Succinimido 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylate

https://huagongshe.com/reaction/265082

反応式

関与物質

役割名称HCID仕込み量
反応物N-HydroxysuccinimideHCID 80170—
反応物1-[(2'-t-Butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylic acidHCID 19036119—
溶媒TetrahydrofuranHCID 8028—
生成物Succinimido 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylateHCID 1903623992.7%

反応手順

206 mg of N,N-dicyclohexylcarbodiimide were added to a suspension of 464 mg of 1-[(2'-t-butoxycarbonylbiphenyl-4-yl)methyl]-2-butyl-4-hydroxymethylimidazole-5-carboxylic acid (prepared as described in Example 4) and 140 mg of N-hydroxysuccinimide in 10 ml of tetrahydrofuran, and the resulting mixture was stirred at room temperature for 16 hours. At the end of this time, the material which had precipitated was filtered off and the filtrate was concentrated by evaporation under reduced pressure. The concentrate was purified by column chromatography through silica gel, using a 1:15 by volume mixture of methanol and methylene chloride as the eluent, to afford 0.52 g of the title compound as crystals, melting at 107°-109° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05646171
出典データセットuspto-grants-1997_07
ORD IDord-0d3a34ba730c472b93fc571b09b2b8ec
出典メモuspto-grants-1997_07