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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1481116생성일: 2026년 10월 26일

Tetramethyltin → 3-Isoquinolinecarboxylic acid, 4-hydroxy-1-methyl-7-phenoxy-, methyl ester

https://huagongshe.com/reaction/1481116

반응식

참여 물질

역할이름HCID투입량
반응물TetramethyltinHCID 11661—
반응물Methyl 1-bromo-4-hydroxy-7-phenoxyisoquinoline-3-carboxylateHCID 89813003—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물3-Isoquinolinecarboxylic acid, 4-hydroxy-1-methyl-7-phenoxy-, methyl esterHCID 7124489558.2%

반응 단계

To a mixture of 1-bromo-4-hydroxy-7-phenoxy-isoquinoline-3-carboxylic acid methyl ester (500 mg, 1.34 mmol) in N-methylpyrrolidone (NMP) (7 mL) was added SnMe4 (358 mg, 2.0 mmol) and resin-bound-Pd(PPh3)2Cl2 (Sigma-Aldrich) (1-2 mmol/g) (40 mg, ca. 0.03 mmol). The resultant mixture was stirred in a 130° C. oil bath for 3 h. Reaction mixture was filtered and rinsed with NMP (1 mL). Filtrate was poured into water (120 mL) and stirred at room temperature until good precipitate formed. Solid was collected and rinsed with water (100 mL) and then hexanes (50 mL). Solid was dried and purified by silica gel chromatography, eluting with 2-50% EtOAc/hexanes, to provide the title compound 240 mg (0.78 mmol) in 58% yield. 1H NMR (200 MHz) CDCl3, δ in ppm: 11.68 (s, 1H), 8.37 (d, J=9.3 Hz, 1H), 7.48-7.08 (m, 7H), 4.07 (s, 3H), 2.75 (s, 3H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409892B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-962b33ddd8fe4c9894890c285bb31bdf
출처 메모uspto-grants-2016_08