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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85448생성일: 2026년 10월 23일

Cesium carbonate → Methyl 6-(4-(dimethylamino)piperidin-1-yl)-1-isopropyl-1H-indazole-4-carboxylate

https://huagongshe.com/ko/reaction/85448

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물N,N-Dimethylpiperidin-4-amineHCID 417391—
반응물Binap, (A+-)-HCID 634876—
반응물Methyl 6-bromo-1-isopropyl-1H-indazole-4-carboxylateHCID 67464993—
촉매Bis(dibenzylideneacetone)palladiumHCID 9811564—
용매MethanolHCID 887—
용매TolueneHCID 1140—
생성물Methyl 6-(4-(dimethylamino)piperidin-1-yl)-1-isopropyl-1H-indazole-4-carboxylateHCID 6821025325%

반응 조건

온도115 °C

반응 단계

To a 10-mL microwave tube were added methyl 6-bromo-1-(1-methylethyl)-1H-indazole-4-carboxylate (200 mg, 0.673 mmol), N,N-dimethyl-4-piperidinamine (95 mg, 0.740 mmol), toluene (3 mL), and cesium carbonate (329 mg, 1.010 mmol), and the mixture was degassed for 5 min by bubbling N2. BINAP (62.9 mg, 0.101 mmol) and Pd2(dba)3 (30.8 mg, 0.034 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 58 mg of product as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.45 (d, J=8.0 Hz, 6H), 1.54-1.61 (m, 2H), 1.87-1.96 (m, 2H), 2.31 (m, 6H), 2.80-2.83 (m, 2H), 3.83-3.86 (m, 2H), 3.93 (s, 3H), 4.98-5.04 (m, 1H), 7.29 (s, 1H), 7.57 (s, 1H), 8.17 (s, 1H). LCMS: (M+H)+=345.2

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846935B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-df772e9d080b431c90e0237028f1cfbd
출처 메모uspto-grants-2014_09