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HRID 1085688作成日:2026年10月27日

Potassium Iodide → N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamine

https://huagongshe.com/reaction/1085688

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium IodideHCID 4875—
反応物Sodium CarbonateHCID 10340—
反応物2-(4-Methoxyphenyl)ethyl methanesulfonateHCID 277977—
反応物N-(4-piperidinyl)-2-benzothiazolamine dihydrobromideHCID 14575275—
溶媒DimethylformamideHCID 6228—
生成物N-[1-[2-(4-methoxyphenyl)ethyl]-4-piperidinyl]-2-benzothiazolamineHCID 1457576441%

反応条件

温度70 °C

反応手順

A mixture of 2.3 parts of [2-(4-methoxyphenyl)ethyl] methanesulfonate, 4 parts of N-(4-piperidinyl)-2-benzothiazolamine dihydrobromide, 5.3 parts of sodium carbonate, 0.1 parts of potassium iodide and 90 parts of N,N-dimethylformamide was stirred overnight at 70° C. The reaction mixture was poured onto water and the product was extracted with methylbenzene. The extract was washed with water, dried, filtered and evaporated. The residue was crystallized from a mixture of 2-propanol and 2,2'-oxybispropane. The product was filtered off and dried, yielding 1.5 parts (41%) of N-[1-[2-(4-methoxyphenyl)-ethyl]-4-piperidinyl]-2-benzothiazolamine; mp. 142.5° C. (178).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05010198
出典データセットuspto-grants-1991_04
ORD IDord-2b99b01b32df4e46b27ab0a7d10c157d
出典メモuspto-grants-1991_04