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HRID 52316作成日:2026年10月26日

4-(Methylsulfonyl)aniline → HCID 178491240、化合物

https://huagongshe.com/reaction/52316

反応式

関与物質

役割名称HCID仕込み量
反応物4-(Methylsulfonyl)anilineHCID 79617—
反応物3-Fluoro-4-methoxybenzonitrileHCID 2774548—
反応物TrimethylaluminumHCID 16682925—
溶媒TolueneHCID 1140—
溶媒ChloroformHCID 6212—
生成物HCID 178491240HCID 178491240—

反応手順

To a suspension of 4-(methylsulfonyl)aniline (2.82 g, 16.5 mmol) in toluene (150 mL), trimethylaluminum (2M solution in toluene, 12.5 mL, 24.7 mmol) was added over 15 minutes. The reaction mixture was warmed to room temperature and stirred for 2.5 hours. A solution of 3-fluoro-4-methoxybenzonitrile (5 g, 33 mmol) in toluene (100 mL) was added over 10 minutes and the reaction mixture was heated to 80°-85° C. After 20 hours, the reaction mixture was cooled to room temperature and poured over a slurry of silica gel in chloroform. After filtration, the reside was washed with a mixture of methylene chloride/methanol (2/1). The combined filtrates were concentrated in vacuo and the resulting yellowish solid was stirred with a mixture of hexane/ether (2/1, 1000 mL). The intermediate was filtered and washed with more hexane/ether (2/1). The pale yellow solid 3-fluoro-4-methoxy-N-[4-(methylsulfonyl)phenyl]benzenecarboximidamide (3.95 g, 74%) was used in the next reaction without further purification: mp (DSC) 195° C. Anal. Calc'd. for C15H15N2SO3F: C, 55.89, H, 4.69, N, 8.69. Found: C, 55.92, H, 4.74, N, 8.53.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05616601
出典データセットuspto-grants-1997_04
ORD IDord-4f3accbe569b48688531b22fb862f88a
出典メモuspto-grants-1997_04