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HRID 51310作成日:2026年10月26日

[9-Benzyl-4-carbamoyl-7-methoxy-1,2,3,4-tetrahydrocarbazol-5-yl]oxyacetic acid sodium salt → [9-Benzyl-4-carbamoyl-7-methoxycarbazol-5-yl]oxyacetic acid

https://huagongshe.com/reaction/51310

反応式

関与物質

役割名称HCID仕込み量
反応物[9-Benzyl-4-carbamoyl-7-methoxy-1,2,3,4-tetrahydrocarbazol-5-yl]oxyacetic acid sodium saltHCID 23676539—
触媒PalladiumHCID 23938—
溶媒Diethylene Glycol Monoethyl EtherHCID 8146—
生成物[9-Benzyl-4-carbamoyl-7-methoxycarbazol-5-yl]oxyacetic acidHCID 10135839—

反応手順

A mixture of 430 mg. of the product from Example 3 Part D, 2.0 gm. of 5% Pd/C, and 20 mL of carbitol was heated to reflux and refluxed for 21 hours, cooled, and filtered. The filtrate was diluted with water, acidified with hydrochloric acid, and extracted well with ethyl acetate. The organic phase was washed with brine, dried over sodium sulfate and evaporated in vacuo. The residue was triturated with dichloromethane and filtered to remove solid tetrahydrocarbazole. The filtrate was evaporated in vacuo to give the title product, 125 mg, 31%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06713645B1
出典データセットuspto-grants-2004_03
ORD IDord-1987d5e7313946f0bcb447800840db56
出典メモuspto-grants-2004_03