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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 85452생성일: 2026년 10월 24일

Morpholine → 1-isopropyl-6-morpholino-1H-indazole-4-carboxylic acid

https://huagongshe.com/ko/reaction/85452

반응식

참여 물질

역할이름HCID투입량
반응물MorpholineHCID 8083—
반응물Sodium t-butoxideHCID 23676156—
반응물Methyl 6-bromo-1-isopropyl-1H-indazole-4-carboxylateHCID 67464993—
촉매Pd XPhos precatalystHCID 131731914—
용매1,4-DioxaneHCID 31275—
생성물1-isopropyl-6-morpholino-1H-indazole-4-carboxylic acidHCID 6746828247.3%

반응 조건

온도98 °C

반응 단계

In a 25 mL sealable tube under nitrogen were combined methyl 6-bromo-1-(1-methylethyl)-1H-indazole-4-carboxylate (250 mg, 0.84 mmol), sodium tert-butoxide (178 mg, 1.85 mmol), Pd-XPhos precatalyst (chloro(2-dicyclohexylphosphino-2′,4′,6′-tri-i-propyl-1,1′-biphenyl) [2-(2-aminoethyl)phenyl]Pd(II); Me-t-butylether adduct) (34.8 mg, 0.042 mmol) and morpholine (81 mg, 0.93 mmol) in Dioxane (4 mL). The resulting mixture was degassed with nitrogen for 10 minutes. The vessel was sealed and the mixture was heated at 98° C. for 20 hours. The contents were diluted with water and 1N HCl was added to adjust the pH˜3-4. The contents were extracted with EtOAc and DCM/isopropanol (8:2), and the combined organic layers were washed with brine, dried over MgSO4, filtered and concentrated. The residue was dissolved in DCM and purified by SiO2 chromatography (eluent: Hexanes/EtOAc gradient 0 to 100% EtOAc). Fractions were evaporated and solids were dried to afford the title compound as a light yellow solid (115 mg, 46%). LC-MS (ES) m/z=290.2. 1H NMR (400 MHz, DMSO-d6) δ ppm 13.13 (br. s., 1H) 8.18 (s, 1H) 7.56 (d, J=2.02 Hz, 1H) 7.26-7.29 (m, 1H) 5.00 (quin, J=6.57 Hz, 1H) 3.77-3.81 (m, 4H) 3.22-3.26 (m, 4H) 1.46 (s, 3H) 1.44 (s, 3H)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08846935B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-157007e98a8f4c6eab9716e8a2574c5e
출처 메모uspto-grants-2014_09