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HRID 934作成日:2026年10月23日

Water → cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide

https://huagongshe.com/ja/reaction/934

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium HydroxideHCID 14797—
反応物cis-N-(1-ethoxycarbonyl-3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 69232225—
溶媒IsopropanolHCID 3776—
生成物cis-N-(3-Methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamideHCID 6923214516.3%

反応手順

2.50 g of the cis-N-(1-ethoxycarbonyl-3-methoxy-4-piperidinyl)-4-amino-5-chloro-2-((S)-1-methyl-2-butynyl)oxybenzamide prepared in the Example 7 and 4.5 g of potassium hydroxide were dissolved in 2-propanol. The obtained solution was refluxed for 1.5 hours and cooled, followed by the addition thereto of water. The resulting mixture was extracted with 10% 2-propanol/chloroform thrice. The combined organic phases were dried over magnesium sulfate and freed from the solvent. The residue was purified by silica gel column chromatography (5 to 12% methanol/dichloromethane) to give 0.34 g of the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05723472
出典データセットuspto-grants-1998_03
ORD IDord-dd08297f1095466ea20b3117b6f50645
出典メモuspto-grants-1998_03