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HRID 390102作成日:2026年10月24日

Methanesulfonyl chloride → N-(3-(6-chloro-4-iodopyridin-2-ylamino)cyclohexyl)methanesulfonamide

https://huagongshe.com/ja/reaction/390102

反応式

関与物質

役割名称HCID仕込み量
反応物Methanesulfonyl chlorideHCID 31297—
反応物N1-(6-chloro-4-iodopyridin-2-yl)cyclohexane-1,3-diamineHCID 86649873—
溶媒PyridineHCID 1049—
生成物N-(3-(6-chloro-4-iodopyridin-2-ylamino)cyclohexyl)methanesulfonamideHCID 87178324—

反応手順

To a solution of EXAMPLE 11A (100 mg, 0.3 mmol) in pyridine (5 mL) was added methanesulfonyl chloride (50 mg, 0.4 mmol). The mixture was stirred at ambient temperature for 5 h and partitioned between ethyl acetate and brine. The organic phase was washed with brine and concentrated. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate to provide the title compound. Yield: 100 mg (82%). MS (DCI/NH3) m/z 430 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08383624B2
出典データセットuspto-grants-2013_02
ORD IDord-9a914a045aa04c59866671a9903bff04
出典メモuspto-grants-2013_02