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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423294생성일: 2026년 10월 24일

Dimethylformamide → 5-(3-Chloro-4-isopropoxyphenyl)-3-(1H-indol-5-yl)-1,2,4-oxadiazole

https://huagongshe.com/ko/reaction/423294

반응식

참여 물질

역할이름HCID투입량
반응물DimethylformamideHCID 6228—
반응물1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물3-Chloro-4-(propan-2-yloxy)benzoic acidHCID 22597728—
생성물5-(3-Chloro-4-isopropoxyphenyl)-3-(1H-indol-5-yl)-1,2,4-oxadiazoleHCID 59318353—

반응 조건

온도80 °C

반응 단계

D4 (7.55 g), HOBT (5.23 g) and EDCI (7.42 g) were dissolved in DMF (88 ml). This mixture was stirred for 10 minutes and then the yellow-orange solid from above (6.16 g) dissolved in DMF (88 ml) was added. The reaction mixture was heated to 80° C. overnight then evaporated and partitioned between EtOAc and H2O. The phases were separated and the aqueous solution extracted with two further portions of EtOAc. The combined organic solutions were dried and evaporated. Part of the crude residue was purified on a 40+M Biotage cartridge, eluting with a 5-30% mixture of EtOAc in hexane. This gave the title compound (1.45 g) as an off-white solid. δH (CDCl3, 400 MHz): 1.45 (6H, d), 4.72 (1H, septet), 6.66-6.69 (1H, m), 7.06 (1H, d), 7.29 (1H, apparent triplet or dd), 7.50 (1H, d), 8.01 (1H, dd), 8.08 (1H, dd), 8.27 (1H, d), 8.49-8.52 (1H, m). MS (ES): C19H16ClN3O2 requires 353; found 354 (MH+). The remaining crude reside was triturated with cold MeOH to give the title compound (3.54 g) as an off white solid. MS data as above.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101775B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-1bae2ca04aba4e5c932bad7e9d2092a3
출처 메모uspto-grants-2012_01