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HRID 6487作成日:2026年10月23日

Methyl 4-(bromomethyl)benzoate → N-[{1-[(4-Carboxyphenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}methyl]-beta-(2-thienyl)alanine

https://huagongshe.com/ja/reaction/6487

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 4-(bromomethyl)benzoateHCID 256687—
反応物L-Phenylalanine, methyl esterHCID 736234—
反応物Sodium borohydrideHCID 4311764—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物(S)-Methyl 2-amino-3-(thiophen-2-yl)propanoateHCID 10899351—
反応物2-n-butyl 4-chloro 1-(2-chlorophenyl)methyl-5-hydroxymethyl-1H-imidazoleHCID 13074095—
反応物N-[{1-[(2 chlorophenyl)methyl]-2-n-butyl-4-chloro-1H-imidazol-5-yl}methyl]phenylalanineHCID 53988647—
生成物N-[{1-[(4-Carboxyphenyl)methyl]-2-n-butyl-1H-imidazol-5-yl}methyl]-beta-(2-thienyl)alanineHCID 44316969—

反応手順

The title compound was prepared following the procedure of Example 3 [(i) method B and (ii)] replacing 2-chlorobenzyl bromide with 4-carbomethoxybenzyl bromide, phenylalanine methyl ester with β-(2-thienyl)alanine methyl ester and sodium cyanoborohydride with sodium borohydride; mp 151°-152° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05248689
出典データセットuspto-grants-1993_09
ORD IDord-7b615b850a714ed28667ec5cac687e9c
出典メモuspto-grants-1993_09