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HRID 68682作成日:2026年10月26日

Diisopropylethylamine → tert-butyl 3-(3-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)ureido)pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/68682

反応式

関与物質

役割名称HCID仕込み量
反応物DiisopropylethylamineHCID 81531—
反応物TriphosgeneHCID 94429—
反応物1-Boc-3-aminopyrrolidineHCID 2756370—
反応物3-(methylthio)-1-phenyl-1H-indazol-6-amineHCID 49839977—
溶媒DichloromethaneHCID 6344—
生成物tert-butyl 3-(3-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)ureido)pyrrolidine-1-carboxylateHCID 67448228—

反応条件

温度0 °C

反応手順

Into a 50-mL 3-necked round-bottom flask, was placed a solution of bis(trichloromethyl)carbonate (200 mg, 0.67 mmol) in dichloromethane (3 mL). To the resulting mixture was then added a mixture of 3-(methylthio)-1-phenyl-1H-indazol-6-amine (500 mg, 1.96 mmol, 1.00 equiv) and DIEA (560 mg, 4.33 mmol, 2.21 equiv) in dichloromethane (2 mL) dropwise with stirring at 0° C. in 30 min. The resulting solution was stirred for 3 h at 15° C. The resulting mixture was added to a solution of tert-butyl 3-aminopyrrolidine-1-carboxylate (440 mg, 2.37 mmol, 1.21 equiv) in dichloromethane (3 mL) dropwise with stirring at 15° C. in 15 min. The resulting solution stirred for an additional 4 h at 15° C. The resulting mixture was concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate:petroleum ether (1:4˜1:3) to yield tert-butyl 3-(3-(3-(methylthio)-1-phenyl-1H-indazol-6-yl)ureido)pyrrolidine-1-carboxylate as a white solid. MS: 468 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08822447B2
出典データセットuspto-grants-2014_09
ORD IDord-64c5866a5fbc4a87a594f9858b5d8e92
出典メモuspto-grants-2014_09