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HRID 85450作成日:2026年10月26日

Nitrogen → Methyl 6-(4-((dimethylamino)methyl)piperidin-1-yl)-1-isopropyl-1H-indazole-4-carboxylate

https://huagongshe.com/reaction/85450

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物Cesium carbonateHCID 10796—
反応物Binap, (A+-)-HCID 634876—
反応物4-(Dimethylaminomethyl)piperidineHCID 11137268—
反応物Methyl 6-bromo-1-isopropyl-1H-indazole-4-carboxylateHCID 67464993—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒MethanolHCID 887—
溶媒TolueneHCID 1140—
生成物Methyl 6-(4-((dimethylamino)methyl)piperidin-1-yl)-1-isopropyl-1H-indazole-4-carboxylateHCID 6746841111.6%

反応条件

温度115 °C

反応手順

To a 10-mL microwave tube were added methyl 6-bromo-1-(1-methylethyl)-1H-indazole-4-carboxylate (250 mg, 0.841 mmol), N,N-dimethyl-1-(4-piperidinyl)methanamine (132 mg, 0.925 mmol), Toluene (3 mL), and cesium carbonate (411 mg, 1.262 mmol), and the mixture was degassed for 5 min by bubbling N2 through BINAP (79 mg, 0.126 mmol) and Pd2(dba)3 (38.5 mg, 0.042 mmol) were added. The tube was sealed and the mixture was heated at 115° C. with stirring for 15 h. The mixture was diluted with methanol (5 mL) and filtered. The filtrate was concentrated and the residue was purified using reverse-phase HPLC to give 35 mg of product as a off-white solid. LCMS MH+=359.3

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846935B2
出典データセットuspto-grants-2014_09
ORD IDord-8419e21f691849a0a468bc7caa513bac
出典メモuspto-grants-2014_09