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HRID 32592作成日:2026年10月26日

3-Aminopyrrolidine → 2-[1-(Cyclohexylmethyl)-4-phenyl-1H-imidazol-5-yl]-7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidine

https://huagongshe.com/reaction/32592

反応式

関与物質

役割名称HCID仕込み量
反応物3-AminopyrrolidineHCID 164401—
反応物7-(Methylthio)[1,3]thiazolo[5,4-d]pyrimidine-2-carbaldehydeHCID 17965798—
反応物4-Aminothieno[2,3-d]pyrimidine-6-carbaldehydeHCID 17965819—
反応物1-(cyclohexylmethyl)-4,5-diphenyl-1H-imidazoleHCID 69194873—
生成物2-[1-(Cyclohexylmethyl)-4-phenyl-1H-imidazol-5-yl]-7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidineHCID 69194440—

反応手順

The title compound was prepared by a similar process to that described for Example 65 but using 7-(methylthio)[1,3]thiazolo[5,4-d]pyrimidine-2-carbaldehyde (Intermediate 77) in place of 4-aminothieno[2,3-d]pyrimidine-6-carbaldehyde (Intermediate 73) and using cyclohexamethylamine in place of 3-aminopyrrolidine. Yellow solid (542 mg) (the product contained 33% of 1-(cyclohexylmethyl)-4,5-diphenyl-1H-imidazole but was used in subsequent steps without further purification);

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07427616B2
出典データセットuspto-grants-2008_09
ORD IDord-cd391bac60304d50bd71986e166b797d
出典メモuspto-grants-2008_09