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HRID 366182生成日期:2026年10月23日

三氟乙酸 → 3-(2-(Methyl-((1R)-1-(methyl-((1R)-1-(methylcarbamoyl)-2-phenylethyl)carbamoyl)-2-(2-naphthyl)ethyl)carbamoyl)vinyl)azetidine-1-carboxylic acid tert-butyl ester

https://huagongshe.com/zh-CN/reaction/366182

反应方程式

参与物

角色名称HCID投料
反应物三氟乙酸HCID 6422—
反应物Carbonic acid sodium salt (1:2)HCID 10340—
反应物碳酸氢三钠HCID 10791—
反应物3-((E)-2-(methyl((1R)-1-(methyl((1R)-1-(methylcarbamoyl)-2-phenylethyl)carbamoyl)-2-(2-naphthyl)ethyl)carbamoyl)vinyl)azetidine-1-carboxylic acid tert-butyl esterHCID 59057257—
溶剂二氯甲烷HCID 6344—
产物3-(2-(Methyl-((1R)-1-(methyl-((1R)-1-(methylcarbamoyl)-2-phenylethyl)carbamoyl)-2-(2-naphthyl)ethyl)carbamoyl)vinyl)azetidine-1-carboxylic acid tert-butyl esterHCID 5382831664.8%

反应步骤

3-((E)-2-(Methyl((1R)-1-(methyl-((1R)-1-(methylcarbamoyl)-2-phenylethyl)-carbamoyl)-2-(2-naphthyl)ethyl)carbamoyl)vinyl)azetidine-1-carboxylic acid tert-butyl ester (0.45 g; 0.73 mmol) was dissolved in methylene chloride (2 mL). Trifluoroacetic acid (2 mL) was added and the reaction mixture was stirred for 7 min. Methylene chloride (50 mL), an aqueous solution of sodium hydrogen carbonate/sodium carbonate (50 mL; pH 9) and sodium carbonate were added to the reaction mixture until pH 8. The organic phase was dried (magnesium sulfate) and evaporated in vacuo to afford 0.29 g of the title compound.

来源与证据

DOI10.6084/m9.figshare.5104873.v1
专利号US06127391
来源数据集uspto-grants-2000_10
ORD IDord-447005111cda44d7b0aa6d32c1add834
来源说明uspto-grants-2000_10