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HRID 551425作成日:2026年10月27日

Carbonate Ion → 1-Phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amine

https://huagongshe.com/reaction/551425

反応式

関与物質

役割名称HCID仕込み量
反応物Carbonate IonHCID 19660—
反応物Sodium SulfateHCID 24436—
反応物Bismuth trichlorideHCID 24591—
反応物DiisopropylethylamineHCID 81531—
反応物(2-(Trifluoromethyl)oxiran-2-yl)methyl 4-methylbenzenesulfonateHCID 24809749—
反応物1-phenyl-1H-indazol-4-amineHCID 24938057—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
溶媒TetrahydrofuranHCID 8028—
生成物1-Phenyl-N-{[2-(trifluoromethyl)-2-oxiranyl]methyl}-1H-indazol-4-amineHCID 2493805356.8%

反応手順

Bismuth chloride (623 mg, 1.98 mmol) was added to a suspension of [2-(trifluoromethyl)-2-oxiranyl]methyl 4-methylbenzenesulfonate (5.85 g, 19.76 mmol) and 1-phenyl-1H-indazol-4-amine (4.13 g, 19.76 mmol) in dry dichloromethane (8 ml) and the mixture stirred at room temperature over the weekend. The resulting thick suspension was diluted with dichloromethane and stirred overnight. The mixture was then diluted with chloroform (200 ml) and sodium sulphate (30 g) and polymer supported carbonate resin (Fluka, ca. 3.5 mmoles carbonate/g resin, 11 g) were added and the mixture stirred overnight. LCMS showed no evidence for cyclisation to the target epoxide. Dry tetrahydrofuran (50 ml) and N,N-diisopropylethylamine (0.85 ml, 4.88 mmol) were then added and the mixture stirred overnight when LCMS indicated complete reaction. The mixture was filtered and the filtrate was washed with water. The aqueous phase was back-extracted with dichloromethane and the combined organic phases were dried and evaporated to give crude product which was purified by silica gel chromatography using the Flashmaster II (2×100 g cartridges) eluting with a 0 to 50% dichloromethane:ethyl acetate gradient over 40 minutes to give the title compound (3.74 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07947727B2
出典データセットuspto-grants-2011_05
ORD IDord-8ffb26c219254c14a3bd6cb2cf47a1ae
出典メモuspto-grants-2011_05