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HRID 649329作成日:2026年10月26日

Hydrochloric Acid → 3,4-Dihydro-2-(3,4-dimethoxyphenyl)-4-methyl-2-[4-(N-methyl-3,4,5-trimethoxyphenethylamino)butyl]-3-oxo-2H-1,4-benzothiazine oxalate

https://huagongshe.com/reaction/649329

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Sodium CarbonateHCID 10340—
反応物N-MethylmescalineHCID 138365—
反応物2-(4-Bromobutyl)-3,4-dihydro-2-(3,4-dimethoxyphenyl)-4-methyl-3-oxo-2H-1,4-benzothiazineHCID 20143035—
溶媒ChloroformHCID 6212—
溶媒DimethylformamideHCID 6228—
生成物3,4-Dihydro-2-(3,4-dimethoxyphenyl)-4-methyl-2-[4-(N-methyl-3,4,5-trimethoxyphenethylamino)butyl]-3-oxo-2H-1,4-benzothiazine oxalateHCID 20143153131.5%

反応手順

To a stirred solution of 2-(4-bromobutyl)-3,4-dihydro-2-(3,4-dimethoxyphenyl)-4-methyl-3-oxo-2H-1,4-benzothiazine (1.5 g, compound No. 32) in dimethylformamide (20 ml), sodium carbonate (0.7 g) and N-methyl-3,4,5-trimethoxyphenethylamine (1.1 g) are added, and the mixture is stirred for 1 hour at 80°-90° C. The mixture is poured into a mixture of chloroform and 1N hydrochloric acid, and the organic layer is concentrated in vacuo. The residue is treated by the similar method as in Example 24 to give 1.5 g (65.8%) of the titled compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04739050
出典データセットuspto-grants-1988_04
ORD IDord-c7979a61fff84202b2ed9906397a15ad
出典メモuspto-grants-1988_04