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HRID 75680作成日:2026年10月23日

Triethylamine → tert-butyl 5-(1-phenyl-1H-tetrazol-5-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate

https://huagongshe.com/ja/reaction/75680

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物1H-Tetrazole, 5-chloro-1-phenyl-HCID 84262—
反応物Tert-butyl octahydropyrrolo(3,4-c)pyrrole-2-carboxylateHCID 4142526—
溶媒1,4-DioxaneHCID 31275—
生成物tert-butyl 5-(1-phenyl-1H-tetrazol-5-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylateHCID 71285583—

反応条件

温度115 °C

反応手順

Et3N (5 mL) was added into a solution of tert-butyl hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate (1 g) and 5-chloro-1-phenyl-1H-tetrazole (1 g) in dioxane (50 mL). The mixture was heated to 115° C. for 24 hours. The reaction was quenched with water (50 mL). The aqueous layer was extracted with EtOAc (3×50 mL). The combined organic phase was dried over MgSO4 and concentrated to give a residue which was purified by silica gel chromatography to give tert-butyl 5-(1-phenyl-1H-tetrazol-5-yl)hexahydropyrrolo[3,4-c]pyrrole-2(1H)-carboxylate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08835454B2
出典データセットuspto-grants-2014_09
ORD IDord-6e979fb885ae435699149ab8f9ee29c1
出典メモuspto-grants-2014_09