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HRID 508143作成日:2026年10月25日

Sulfuryl chloride → 1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)phenyl]-amide

https://huagongshe.com/reaction/508143

反応式

関与物質

役割名称HCID仕込み量
反応物Sulfuryl chlorideHCID 24648—
反応物1-(Prop-2-en-1-yl)cyclopropane-1-sulfonyl chlorideHCID 44181959—
反応物3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamineHCID 59386343—
溶媒PyridineHCID 1049—
生成物1-Allyl-cyclopropanesulfonic acid [3,4,6-trifluoro-2-(2-fluoro-4-iodo-phenylamino)phenyl]-amideHCID 57626644—

反応条件

温度40 °C

反応手順

To a stirred solution of the amine, i.e., 3,5,6-trifluoro-N1-(2-fluoro-4-iodophenyl)benzene-1,2-diamine, (1 eq) in anhydrous pyridine (5 ml/mmole) was added the sulfonyl chloride, i.e., 1-allyl-cyclopropanesulfonyl chloride, (1-5 eq). The reaction mixture was stirred at 40° C. for 48 hours. The reaction mixture was partitioned with water and EtOAc. The organic layer was washed with brine, dried (MGSO4) and concentrated under reduced pressure. The residue was purified by flash column chromatography on silica. 1H NMR (CDCl3, 300 MHz): δ 7.41 (dd, 1H), 7.38 (dd, 1H), 7.09 (s, 1H), 6.78 (m, 1H), 6.49 (m, 1H), 5.96 (s, 1H), 5.86 (m, 1H), 5.18 (d, 2H), 2.76 (d, 2H), 1.23 (m, 2H), 0.872 (m, 2H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09095581B2
出典データセットuspto-grants-2015_08
ORD IDord-182caf2807d84ef799efe0560e10dc7d
出典メモuspto-grants-2015_08