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HRID 394271作成日:2026年10月24日

1,3-Dichloroacetone → 4-(Chloromethyl)-2-phenyl-1,3-thiazole

https://huagongshe.com/ja/reaction/394271

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-DichloroacetoneHCID 10793—
反応物ThiobenzamideHCID 683563—
反応物2-Phenyl-4-(beta-hydroxyethyl)thiazoleHCID 10608315—
反応物[Rac]-2-ethoxy-3-(3-fluoro-4-hydroxy-phenyl)-propionic acid ethyl esterHCID 68618019—
生成物4-(Chloromethyl)-2-phenyl-1,3-thiazoleHCID 236969—

反応手順

In analogy to the procedure described in example 1 d], [rac]-2-ethoxy-3-(3-fluoro-4-hydroxy-phenyl)-propionic acid ethyl ester (example 7 a]) was reacted with 2-(2-phenyl-thiazol-4-yl)-ethanol (prepared from thiobenzamide and 1,3-dichloroacetone in analogy to the procedure described in example 4 a] to give 4-chloromethyl-2-phenyl-thiazole followed by side chain elongation in analogy to the sequence described in examples 13 a] to 13 d]) in tetrahydrofuran in the presence of triphenylphosphine and DEAD (diethyl azodicarboxylate) to yield [rac]2-ethoxy-3-{3-fluoro-4-[2-(2-phenyl-thiazol-4-yl)-ethoxy]-phenyl}-propionic acid ethyl ester, which was further saponified in analogy to the procedure described in example 4 e], to yield [rac]2-ethoxy-3-{3-fluoro-4-[2-(2-phenyl-thiazol-4-yl)-ethoxy]-phenyl}-propionic acid as a light yellow gum.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06809110B2
出典データセットuspto-grants-2004_10
ORD IDord-eaa609cebea543ea9fbd5923d28b44cf
出典メモuspto-grants-2004_10