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HRID 1184642作成日:2026年10月27日

Pyridine → {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}hexadecanoate

https://huagongshe.com/reaction/1184642

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物DichloromethaneHCID 6344—
反応物Palmitoyl chlorideHCID 8206—
反応物TolvaptanHCID 216237—
溶媒WaterHCID 962—
生成物{7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}hexadecanoateHCID 8665215174.4%

反応手順

Palmitoyl chloride (1.24 ml, 4.4 mmol) was added to a dichloromethane (20 ml) solution of tolvaptan (2.00 g, 4.4 mmol) and pyridine (0.40 ml, 5.0 mmol), and the mixture was stirred at room temperature over night. Water was added to the reaction mixture and the mixture was extracted with dichloromethane. The combined organic layer was washed with water and an aqueous saturated sodium chloride solution, and dried over magnesium sulfate. After filtration and concentration, the residue was purified by silica gel chromatography (n-hexane:ethyl acetate) to thereby obtain 2.25 g (74%) of {7-chloro-1-[2-methyl-4-(2-methyl-benzoylamino)-benzoyl]-2,3,4,5-tetrahydro-1H-benzo[b]azepin-5-yl}hexadecanoate as amorphous.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08669229B2
出典データセットuspto-grants-2014_03
ORD IDord-9567796359444165a637330ea1574e1c
出典メモuspto-grants-2014_03