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HRID 1032542作成日:2026年10月27日

Methanesulfonyl chloride → N-[4-(2-Dimethylaminoethyl)-1H-indazol-7-yl]methanesulfonamide, Hydrochloride

https://huagongshe.com/reaction/1032542

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N,N-dimethyl-N-[2-(7-amino-1H-indazol-4-yl)ethyl]amineHCID 13629325—
溶媒DimethylformamideHCID 6228—
溶媒TetrahydrofuranHCID 8028—
生成物N-[4-(2-Dimethylaminoethyl)-1H-indazol-7-yl]methanesulfonamide, HydrochlorideHCID 131716572—

反応条件

温度0 °C

反応手順

At 0° C., 1.2 g of N,N-dimethyl-N-[2-(7-amino-1H-indazol-4-yl)ethyl]amine in 10 ml of dimethylformamide and 5 ml of tetrahydrofuran is combined with 0.91 ml of methanesulfonyl chloride The mixture is agitated for 2 hours at 0° C. and for 14 hours at room temperature. The product is chromatographed on silica gel with methanol/dichloromethane 1:1 and treated with ethereal hydrochloric acid, obtaining, after recrystallization from methanol/diethyl ether, 550 mg of N-[4-(2-dimethylamino-ethyl)-1H-indazol-7-yl]methanesulfonamide, hydrochloride, mp 203°-205° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04958026
出典データセットuspto-grants-1990_09
ORD IDord-e67e53afb7fe4fdc9e7d4a7a681f1169
出典メモuspto-grants-1990_09