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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893667생성일: 2026년 10월 25일

4-Chloro-7-methoxycinnoline → HCID 68617576, 화합물

https://huagongshe.com/reaction/1893667

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참여 물질

역할이름HCID투입량
반응물4-Chloro-7-methoxycinnolineHCID 21991021—
반응물Potassium tert-butoxideHCID 23665647—
반응물1-{[1-(2-tert-Butoxycarbonylamino-3,3-dimethylbutyryl)-4-hydroxypyrrolidine-2-carbonyl]-amino}-2-ethyl-cyclopropanecarboxylic acidHCID 68616376—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물HCID 68617576HCID 6861757657%

반응 조건

온도0 °C

반응 단계

To 1-{[1-(2-tert-butoxycarbonylamino-3,3-dimethyl-butyryl)-4-hydroxy-pyrrolidine-2-carbonyl]-amino}-2-ethyl-cyclopropanecarboxylic acid (210 mmg, 0.46 mmol) at 0° C. (external temperature, ice bath) was added KOt-Bu (1 m in THF, 2.3 mL, 2.3 mmol, 5 equiv.) and 4-chloro-7-methoxy-cinnoline (95 mg, 0.49 mmol, 1.06 equiv.) in THF (3 mL). The reaction was stirred at 0° C. for 2.5 h and diluted with EtOAc. The solution was washed with aqueous HCl (1M), resulting a precipitation of the crude product. The organic layer was dried over Na2SO4 and combined with the precipitate. The crude product was purified by column chromatography (0→15% MeOH/CH2Cl2) to provide 1-{[1-(2-tert-butoxycarbonylamino-3,3-dimethyl-butyryl)-4-(7-methoxy-cinnolin-4-yloxy)-pyrrolidine-2-carbonyl]-amino}-2-ethyl-cyclopropanecarboxylic acid (161 mg, 57%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513186B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-eab50754a6f44ebb9afd4caa9feb927f
출처 메모uspto-grants-2013_08