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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 253251생성일: 2026년 10월 26일

Trifluoroacetic acid → HCID 178496062, 화합물

https://huagongshe.com/reaction/253251

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물3-Chloro-4-hydroxybenzaldehydeHCID 17022—
반응물HCID 178496107HCID 178496107—
용매MethanolHCID 887—
생성물HCID 178496062HCID 17849606247.2%

반응 조건

온도70 °C

반응 단계

A mixture of 4-(3,4-bis{[2-(methyloxy)ethyl]oxy}phenyl)-3-methyl-1H-pyrazol-5-amine (114 mg, 0.36 mmol), 3-chloro-4-hydroxybenzaldehyde (117 mg, 0.75 mmol) and trifluoroacetic acid (3 mL) was heated at 70° C. for 18 hours. Then the reaction mixture was concentrated, dissolved in 10 mL of N,N-dimethylformamide and purified by preparatory HPLC (Shimadzu LC-8A HPLC, Waters Xterra C18 30 mm×100 mm column, acetonitrile-water-trifluoroacetic eluent). After concentration then lyophillization of the pure fractions a yellow powder was obtained. It was dissolved in 4 mL of 1:1 methanol: 4M hydrogen chloride in dioxane, and evaporated to dryness (repeated three times) to give 2-chloro-4-(1-methyl-7,8-bis{[2-(methyloxy)ethyl]oxy}-3H-pyrazolo[3,4-c]isoquinolin-5-yl)phenol hydrochloride salt (84 mg, 0.17 mmol, 47% yield) 1H NMR (400 MHz, d6-DMSO): 10.65 (b, 1H), 7.68-7.67 (b, 2H), 7.53-7.48 (m, 2H), 7.16-7.14 (d, 1H), 4.45-4.43 (m, 2H), 4.09-4.07 (m, 2H), 3.80-3.78 (m, 2H), 3.68-3.66 (m, 2H), 3.36 (s, 3H), 3.30 (s, 3H), 2.81 (s, 3H); MS (EI) for C23H24ClN3O5: 458 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07872014B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-83700b6e03a9487f9df0f782d8d0efd2
출처 메모uspto-grants-2011_01