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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 38873생성일: 2026년 10월 23일

Cyclohexanemethanol → {5-[6-(1H-Indol-4-yl)-1H-indazol-4-yl]-1,3,4-oxadiazol-2-yl}methanol

https://huagongshe.com/ko/reaction/38873

반응식

참여 물질

역할이름HCID투입량
반응물CyclohexanemethanolHCID 7507—
반응물Potassium CarbonateHCID 11430—
반응물4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazoleHCID 66776954—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물{5-[6-(1H-Indol-4-yl)-1H-indazol-4-yl]-1,3,4-oxadiazol-2-yl}methanolHCID 6669192229.6%

반응 조건

온도100 °C

반응 단계

4-[5-(Chloromethyl)-1,3,4-oxadiazol-2-yl]-6-(1H-indol-4-yl)-1-(phenylsulfonyl)-1H-indazole (25 mg, 0.051 mmol), cyclohexylmethanol (17.48 mg, 0.153 mmol) and potassium carbonate (21.16 mg, 0.153 mmol) were placed in N-methyl-2-pyrrolidone (1 ml) and the mixture heated under microwave irradiation at 100° C. for 20 mins. Additional cyclohexylmethanol (17.48 mg, 0.153 mmol) was added and the mixture heated at 110° C. for 20 mins, followed by 110° C. for a further 20 mins. The solvent was removed and the residue purified by Mass Directed Automated Preparative HPLC to give the title compound as a white solid (5 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08524751B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-a8aed5489aee458d9214f40f1d9238cf
출처 메모uspto-grants-2013_09