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HRID 376305作成日:2026年10月27日

Sodium Azide → (4-Azidomethyl-4-fluoro-piperidin-1-yl)-(3-chloro-4-fluoro-phenyl)methanone

https://huagongshe.com/reaction/376305

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium AzideHCID 33557—
反応物1-Butanaminium, N,N,N-tributyl-, azideHCID 5743232—
反応物toluene-4-sulfonic acid 1-(3-chloro-4-fluorobenzoyl)-4-fluoropiperidin-4-yl-methyl EsterHCID 10718129—
溶媒Dimethyl SulfoxideHCID 679—
生成物(4-Azidomethyl-4-fluoro-piperidin-1-yl)-(3-chloro-4-fluoro-phenyl)methanoneHCID 19361720—

反応条件

温度110 °C

反応手順

0.70 g of toluene-4-sulfonic acid 1-(3-chloro-4-fluorobenzoyl)-4-fluoropiperidin-4-yl-methyl ester (1.57 mmol), 0.308 g of sodium azide (4.70 mmol) and 0.20 g of tetrabutylammonium azide (0.70 mmol) are mixed in 3.50 ml of dimethyl sulfoxide. The mixture is heated at 110° C. under a nitrogen atmosphere for 20 hours. The reaction mixture is poured into ice-cold water and then extracted with ethyl acetate. The organic phase is washed with water and then with a saturated aqueous solution of sodium chloride, dried over magnesium sulfate, filtered and concentrated under vacuum. The title product is isolated by chromatography on a neutral alumina column (eluent: hexane/ethyl acetate; 70:30). 0.313 g of a yellow oil is obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06020345
出典データセットuspto-grants-2000_02
ORD IDord-96948f1aa17d4d099e8f00b9ae990101
出典メモuspto-grants-2000_02