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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423340생성일: 2026년 10월 24일

1,2-Dichloroethane → Ethyl 3-[4-(5-{5-chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1-yl]propanoate

https://huagongshe.com/ko/reaction/423340

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물5-Chloro-6-isopropoxynicotinic acidHCID 18070582—
반응물HCID 178471833HCID 178471833—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물Ethyl 3-[4-(5-{5-chloro-6-[(1-methylethyl)oxy]-3-pyridinyl}-1,2,4-oxadiazol-3-yl)-1H-indol-1-yl]propanoateHCID 5931839334.7%

반응 조건

온도80 °C

반응 단계

To 5-chloro-6-[(1-methylethyl)oxy]-3-pyridinecarboxylic acid (D61) (1.504 g, 6.97 mmol) in dry DMF (30 ml) was added EDC (1.604 g, 8.37 mmol) and HOBT (1.282 g, 8.37 mmol). Stirred solution at RT for 10 minutes then added ethyl 3-{4-[(hydroxyamino)(imino)methyl]-1H-indol-1-yl}propanoate (N4111-31-A4) (D57) (1.92 g, 6.97 mmol). The mixture was stirred for 30 minutes. LC/MS showed one product (intermediate). The solution was heated at 80° C. for 2 hours. Left standing overnight at RT then heated 80° C. for further 2 hours to give complete reaction. Cooled and added EtOAc (250 ml). The EtOAc was washed with sat. NaHCO3 (150 ml) followed by water (2×200 ml). Dried over MgSO4 and evaporated off the solvent. The residue was subjected to chromatography on the biotage (EtOAc/hexane 1:2). On evaporation of most of the solvent from clean fractions and addition of hexane a white precipitate was formed. The solid was filtered off to obtain 1.1 g of the title product. MS (ES) C23H2335ClN4O4 requires 454; found 455 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101775B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-a10c3b25e48348cb8593b8cd05836e38
출처 메모uspto-grants-2012_01