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HRID 479235作成日:2026年10月25日

4-Chlorobenzaldehyde → [Rac]-3-(7-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-benzo[b]thiophen-4-yl)-2-ethoxy-propionic acid methyl ester

https://huagongshe.com/reaction/479235

反応式

関与物質

役割名称HCID仕込み量
反応物4-ChlorobenzaldehydeHCID 7726—
反応物TriphenylphosphineHCID 11776—
反応物ethyl N-ethoxycarbonyliminocarbamateHCID 220568—
反応物2-[2-(4-Chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanolHCID 22273906—
反応物[Rac]-2-ethoxy-3-(7-hydroxy-benzo[b]thiophen-4-yl)-propionic acid methyl esterHCID 68616696—
生成物[Rac]-3-(7-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-benzo[b]thiophen-4-yl)-2-ethoxy-propionic acid methyl esterHCID 69557571—

反応手順

In analogy to the procedure described in example 17 a], [rac]-2-ethoxy-3-(7-hydroxy-benzo[b]thiophen-4-yl)-propionic acid methyl ester (example 151 a]) was reacted with 2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol (prepared by conversion of the 4-chloro-benzaldehyde into 2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethanol in analogy to the sequence described in examples 21 a] to 21 e]) in the presence of triphenylphosphine and DEAD (diethyl azodicarboxylate) to yield [rac]-3-(7-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-benzo[b]thiophen-4-yl)-2-ethoxy-propionic acid methyl ester, which was further saponified in analogy to the procedure described in example 91 e] to yield [rac]-3-(7-{2-[2-(4-chloro-phenyl)-5-methyl-oxazol-4-yl]-ethoxy}-benzo[b]thiophen-4-yl)-2-ethoxy-propionic acid as colorless oil.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06642389B2
出典データセットuspto-grants-2003_11
ORD IDord-c7d3eef312f843ed8f577cd25a5a761c
出典メモuspto-grants-2003_11