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HRID 225130作成日:2026年10月27日

Water → 2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrate

https://huagongshe.com/reaction/225130

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物3-amino-N-ethylpiperidineHCID 98094—
反応物Bis-(1H-imidazol-2-YL)-methanoneHCID 5250894—
反応物2-[4-(7-Chloro-4-quinolylamino)phenyl]acetic acid hydrochlorideHCID 70597336—
溶媒Dimethyl SulfoxideHCID 679—
生成物2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrateHCID 2332900492.5%

反応条件

温度100 °C

反応手順

7.0 Grams (0.02 mole) of 2-[4-(7-chloro-4-quinolylamino)phenyl]acetic acid hydrochloride were dissolved in 150 milliliters of dimethyl sulphoxide by heating the stirred mixture to 100° C. under nitrogen. The solution was cooled to room temperature, 6.48 grams (0.04 mole) of carbonyl di-imidazole were added and the mixture was stirred for 21/2 hours under nitrogen. 7.68 Grams (0.06 mole) of 3-amino-1-ethylpiperidine were added, the solution was stirred for another 21/2 hours and poured into 500 milliliters of water. The mixture was refrigerated overnight and the resulting solid was broken up, stirred with water, collected and dried. The solid was dissolved in chloroform and chromatographed on an alumina column made up in chloroform. Elution with chloroform/methanol (4:1) gave 8.15 grams (92.5% yield) of 2-[4-(7-chloro-4-quinolylamino)phenyl]-N-(1-ethyl-3-piperidyl)acetamide monohydrate, melting point 160°-162° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04235908
出典データセットuspto-grants-1980_11
ORD IDord-eb994b99a963498aa299fb5d018646e3
出典メモuspto-grants-1980_11