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HRID 244733作成日:2026年10月26日

1-Ethyl-3-methyl-1H-pyrazole-5-carboxylic acid → 1-Ethyl-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-3-methyl-1H-pyrazole-5-carboxamide

https://huagongshe.com/reaction/244733

反応式

関与物質

役割名称HCID仕込み量
反応物1-Ethyl-3-methyl-1H-pyrazole-5-carboxylic acidHCID 2743794—
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—
溶媒DiisopropylethylamineHCID 81531—
生成物1-Ethyl-N-[6-(1H-indol-4-yl)-1H-indazol-4-yl]-3-methyl-1H-pyrazole-5-carboxamideHCID 44540156—

反応手順

1-Ethyl-3-methyl-1H-pyrazole-5-carboxylic acid (67.8 mg) was treated with N-[(dimethylamino)(3H-[1,2,3]triazolo[4,5-b]pyridin-3-yloxy)methylidene]-N-methylmethanaminium hexafluorophosphate (168 mg) in DMF (750 μl) and DIPEA (150 μl). Reaction mixture was shaken for five min prior to treatment with 6-(1H-indol-4-yl)-1H-indazol-4-amine (50 mg) in DMF (350 μl). Reaction mixture was left to stand at 22° C. for 16 hrs. Solvent was removed in vacuo and the product re-dissolved in chloroform (0.3 ml) prior to application on to a preconditioned (methanol then chloroform) aminopropyl SPE cartridge (1 g). Product was eluted after 2 h with ethyl acetate:methanol (1:1, 3.2 ml), and concentrated under a stream of nitrogen using blow down apparatus. Purification by mass directed preparative HPLC (Method B) gave the title compound.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658635B2
出典データセットuspto-grants-2014_02
ORD IDord-5aafeaabfc944540b2cc041bafca5b9a
出典メモuspto-grants-2014_02