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HRID 42250作成日:2026年10月25日

2-Ethoxybenzoic acid → 2-(Ethyloxy)-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]benzamide

https://huagongshe.com/reaction/42250

反応式

関与物質

役割名称HCID仕込み量
反応物2-Ethoxybenzoic acidHCID 67252—
反応物DiisopropylethylamineHCID 81531—
反応物Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
反応物6-(1H-indol-4-yl)-1H-indazol-4-amineHCID 58268019—
溶媒DimethylformamideHCID 6228—
生成物2-(Ethyloxy)-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]benzamideHCID 44540310—

反応手順

To a solution of 2-(ethyloxy)benzoic acid (67 mg, 0.40 mmol) in DMF (1 ml), HATU (248 mg, 0.40 mmol) and DIPEA (0.211 mL, 1.21 mmol) were added. The reaction was stirred for 30 mins under nitrogen before addition of 6-(1H-indol-4-yl)-1H-indazol-4-amine (50 mg, 0.20 mmol). The reaction was stirred overnight then it was loaded onto a PS-aminopropyl cartridge (5 g) and left for 3 h. The cartridge was washed with 10% MeOH in DCM. Appropriate fractions were combined and the solvent was evaporated. The residue was dissolved in MeOH:DMSO (1 ml; 1:1, v/v) and purified by Mass Directed Automated Preparative HPLC using method B. Appropriate fractions were dried under a stream of nitrogen to give title compound, 27 mg.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536169B2
出典データセットuspto-grants-2013_09
ORD IDord-cab91de482c944419f7d48679e95dcd9
出典メモuspto-grants-2013_09