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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1522502생성일: 2026년 10월 27일

Benzene → Ethyl 1-(1,1-dimethylethyl)-3-methyl-6-[4-(methyloxy)phenyl]-1H-pyrazolo[3,4-b]pyridine-4-carboxylate

https://huagongshe.com/reaction/1522502

반응식

참여 물질

역할이름HCID투입량
반응물BenzeneHCID 241—
반응물Ethyl 4-(4-methoxyphenyl)-2,4-dioxobutanoateHCID 287267—
반응물1-tert-Butyl-3-methyl-1H-pyrazol-5-amineHCID 737200—
용매Acetic AcidHCID 176—
생성물Ethyl 1-(1,1-dimethylethyl)-3-methyl-6-[4-(methyloxy)phenyl]-1H-pyrazolo[3,4-b]pyridine-4-carboxylateHCID 67124416—

반응 단계

The title compound was prepared in the same manner as described for intermediate 61 using ethyl 4-[4-(methyloxy)phenyl]-2,4-dioxobutanoate (327 mg, 1.305 mmol), benzene (8 mL), 1-(1,1-dimethylethyl)-3-methyl-1H-pyrazol-5-amine (200 mg, 1.305 mmol), and acetic acid (2 mL). The crude product was purified using column chromatography (Silica gel, eluent: 0 to 100% EtOAc/hexanes) to give 0.41 g (85%) of product. LCMS E-S (M+H)=368.1. 1H NMR (400 MHz, DMSO-d6) δ ppm 1.81 (s, 9 H), 2.55 (s, 3 H), 7.11 (d, J=8.84 Hz, 2 H), 7.89 (s, 1 H), 8.16 (d, J=8.84 Hz, 2 H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09073924B2
출처 데이터셋uspto-grants-2015_07
ORD IDord-3b502d20205a47e39b96305c0309809a
출처 메모uspto-grants-2015_07