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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 423292생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/423292

반응식

참여 물질

역할이름HCID투입량
반응물PyBOPHCID 2724699—
반응물3-Chloro-4-(propan-2-yloxy)benzoic acidHCID 22597728—
반응물HCID 178513238HCID 178513238—
용매DimethylformamideHCID 6228—
생성물5-(3-Chloro-4-isopropoxyphenyl)-3-(1H-indol-5-yl)-1,2,4-oxadiazoleHCID 5931835311.9%

반응 단계

D1 (500 mg), D4 (611 mg) and PyBOP (1.66 g) were dissolved in DMF and stirred overnight. The reaction mixture was then evaporated and partitioned between EtOAc and H2O. The organic layer was washed with H2O (×2) then brine, dried over MgSO4, filtered and evaporated to give the crude product. This was purified on a silica cartridge, eluting with a 0 to 50% mixture of Et2O in hexane to give the title compound (120 mg) as a white solid. δH (CDCl3, 400 MHz): 1.43 (6H, d), 4.69 (1H, septet), 6.92 (1H, s), 7.04 (1H, d), 7.25 (1H, s), 7.48 (1H, d), 8.00 (1H, d), 8.07 (1H, d), 8.25 (1H, s), 8.39 (1H, br. s), 8.50 (1H, s). MS (ES): C19H16ClN3O2 requires 353; found 354 (MH+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08101775B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-4f7805d80bb0444b915b9cd35f8d77b5
출처 메모uspto-grants-2012_01