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HRID 368871作成日:2026年10月26日

4-Fluorobenzenesulfonamide → (S)-(-)-4-[4-[2-(Isochroman-1-yl)ethyl]-cis-3,5-dimethylpiperazin-1-yl]benzenesulfonamide

https://huagongshe.com/reaction/368871

反応式

関与物質

役割名称HCID仕込み量
反応物4-FluorobenzenesulfonamideHCID 120231—
反応物4-(Piperazin-1-yl)benzene-1-sulfonamideHCID 901897—
反応物rel-(2R,6S)-2,6-dimethylpiperazineHCID 6950261—
反応物4-(3,5-Dimethylpiperazin-1-yl)benzenesulfonamideHCID 23288831—
反応物1-(2-Chloroethyl)-4-methyl-isochromanHCID 23288938—
反応物(4S)-4-(phenylmethyl)-3-(2-phenylpropionyl)-2-oxazolidinoneHCID 56980759—
生成物(S)-(-)-4-[4-[2-(Isochroman-1-yl)ethyl]-cis-3,5-dimethylpiperazin-1-yl]benzenesulfonamideHCID 21308103—

反応手順

Following the general procedure of EXAMPLE 49 and making non-critical variations 2-(isochroman-1-yl)ethanol-O-methanesulfonate (LXXX, 0.412 g) and 4-(3,5-dimethylpiperazin-1-yl)benzenesulfonamide [(IV), 0.433 g; prepared from 4-fluorobenzenesulfonamide, III, and cis-2,6-dimethylpiperazine, II (Aldrich), by the method of EXAMPLE 47] gives the title compound; mp 170-175 (decomp)°; MS (m/z) 429; IR (mineral oil) 1153, 1596, 1325, 1162 and 1096 cm-1.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06133446
出典データセットuspto-grants-2000_10
ORD IDord-7e93ca9197244dd48f8f4e64ea4022a5
出典メモuspto-grants-2000_10