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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 877112생성일: 2026년 10월 24일

1,1'-Carbonyldiimidazole → N-Methoxy-N-methyl-1H-indazole-3-carboxamide

https://huagongshe.com/ko/reaction/877112

반응식

참여 물질

역할이름HCID투입량
반응물1,1'-CarbonyldiimidazoleHCID 68263—
반응물Indazole-3-carboxylic acidHCID 78250—
반응물Methanamine, N-methoxy-, hydrochloride (1:1)HCID 81138—
용매DimethylformamideHCID 6228—
생성물N-Methoxy-N-methyl-1H-indazole-3-carboxamideHCID 1603686779%

반응 조건

온도62.5 °C

반응 단계

1H-indazole-3-carboxylic acid (XV) (100 g, 617 mmol) in DMF was treated with carbonyldiimidazole (110 g, 678 mmol) at room temperature until the evolution of gas ceased (ca. 15 minutes). The reaction was heated to 60-65° C. for two hours and then allowed to cool to room temperature. N,O-Dimethylhydroxylamine-HCl (66.2 g, 678 mmol) was added as a solid and the mixture was heated to 65° C. for 3 hours. The reaction was concentrated to a paste and taken up in DCM, and washed subsequently with water and 2N HCl. The product could be seen coming out of solution. The solid was filtered and rinsed separately with EtOAc. The EtOAc and DCM layers were separately washed with sodium bicarbonate followed by brine, dried over MgSO4 and concentrated under reduced pressure. The resulting solids were combined, triturated with 1:1 mixture of DCM-ether, filtered, and dried to produce N-methoxy-N-methyl-1H-indazole-3-carboxamide (XVI) as a white solid (100 g, 487 mmol, 79% yield). 1H NMR (DMSO-d6) δ ppm 3.46 (s, 3H), 3.69-3.85 (m, 3H), 7.13-7.31 (m, 1H), 7.41 (t, J=7.25 Hz, 1H), 7.56-7.65 (m, 1H), 7.93-8.08 (m, 1H); ESIMS found for C10H11N3O2 m/z 206 (M+H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08987298B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-3ad07c6689a14ecaa709441d65075360
출처 메모uspto-grants-2015_03