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HRID 423292作成日:2026年10月27日

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

https://huagongshe.com/reaction/423292

反応式

関与物質

役割名称HCID仕込み量
反応物PyBOPHCID 2724699—
反応物3-Chloro-4-(propan-2-yloxy)benzoic acidHCID 22597728—
反応物HCID 178513238HCID 178513238—
溶媒DimethylformamideHCID 6228—
生成物5-(3-Chloro-4-isopropoxyphenyl)-3-(1H-indol-5-yl)-1,2,4-oxadiazoleHCID 5931835311.9%

反応手順

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+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08101775B2
出典データセットuspto-grants-2012_01
ORD IDord-4f7805d80bb0444b915b9cd35f8d77b5
出典メモuspto-grants-2012_01