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HRID 2073547作成日:2026年10月25日

Methanol → 4[1-(2-Carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoic acid

https://huagongshe.com/reaction/2073547

反応式

関与物質

役割名称HCID仕込み量
反応物MethanolHCID 887—
反応物TetrahydrofuranHCID 8028—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物Methyl 4-[1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoateHCID 19822473—
溶媒WaterHCID 962—
生成物4[1-(2-Carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoic acidHCID 1982246979.2%

反応手順

A solution of methyl 4-[1-(2-carbamoylethyl)-5-(N-cyclopentylmethylcarbamoyl)indol-3-ylmethyl]-3-methoxybenzoate (0.13 g) in a combination of methanol (2 ml), tetrahydrofuran (2 ml), and water (1 ml) was treated with lithium hydroxide monohydrate (0.07 g). The mixture was stirred for 12 hours and then concentrated to remove the organic solvents. The resultant aqueous solution was acidified with 10% (v/v) hydrochloric acid. The white precipitate which formed was collected by filtration, washed with water, and dried under vacuum to give the title compound (0.10 g, 79%) as a white powder; mp 129°-131° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04918094
出典データセットuspto-grants-1990_04
ORD IDord-46e278499ad145f6a176e23a6cb03398
出典メモuspto-grants-1990_04