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HRID 276603作成日:2026年10月23日

1,3-Dioxane, 2-(2-bromoethyl)- → 2-(2-Methyl-4-nitrophenylimino)-1-(2-(1,3-dioxan-2-yl)ethyl)-3-thia-1-azaspiro[4.4]nonane

https://huagongshe.com/ja/reaction/276603

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Dioxane, 2-(2-bromoethyl)-HCID 520656—
反応物2-(2-Methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonaneHCID 178428736—
生成物2-(2-Methyl-4-nitrophenylimino)-1-(2-(1,3-dioxan-2-yl)ethyl)-3-thia-1-azaspiro[4.4]nonaneHCID 18316176—

反応手順

1-Hydroxymethylcyclopentanamine was prepared according to Method B1c. The 2-hydroxyethylamine was converted to 1-chloromethylcyclopentanamine HCl salt according to Method B7e. 1-Chloromethylcyclopentanamine HCl salt was reacted with 2-methyl-4-nitrophenyl isothiocyanate according to Method C1e to give 2-(2-methyl-4-nitrophenylimino)-3-thia-1-azaspiro[4.4]nonane. The thiazolidine was reacted with 2-(2-bromoethyl)-1,3-dioxane according to Method D2e to give 2-(2-methyl-4-nitrophenylimino)-1-(2-(1,3-dioxan-2-yl)ethyl)-3-thia-1-azaspiro[4.4]nonane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06353006B1
出典データセットuspto-grants-2002_03
ORD IDord-60c8c5af40a5465d84358fbdadab9fdc
出典メモuspto-grants-2002_03