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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 600999생성일: 2026년 10월 26일

1,10-Phenanthroline → N-(3-morpholin-4-yl-phenyl)-hydrazinecarboxylic acid tert-butyl ester

https://huagongshe.com/reaction/600999

반응식

참여 물질

역할이름HCID투입량
반응물1,10-PhenanthrolineHCID 1318—
반응물Cesium carbonateHCID 10796—
반응물tert-Butyl carbazateHCID 70091—
반응물4-(3-Iodophenyl)morpholineHCID 54536434—
촉매Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물N-(3-morpholin-4-yl-phenyl)-hydrazinecarboxylic acid tert-butyl esterHCID 5897701862.1%

반응 조건

온도80 °C

반응 단계

To a solution of 4-(3-iodo-phenyl)-morpholine (1.81 g, 6.26 mmol) in DMF (6.5 mL) under nitrogen was added tert-butylcarbazate (993 mg, 7.52 mmol), copper (I) iodide (59.5 mg, 0.313 mmol), 1,10-phenanthroline (113 mg, 0.626 mmol) and cesium carbonate (2.85 g, 8.77 mmol). The mixture was heated at 80° C. for 18 h and then cooled to room temperature. Water (100 mL) was added and the mixture was extracted with ethyl acetate. The organic layer was dried over MgSO4, concentrated. The residue was purified by silica gel column chromatograghy eluted with EtOAc:hexanes (25 to 50% EtOAc) to give N-(3-morpholin-4-yl-phenyl)-hydrazinecarboxylic acid tert-butyl ester (1.14 g, 62%) as a yellowi oil. MS (ES+): m/z=294.2. 1H NMR (DMSO-d6, 500 MHz): δ 1.44 (s, 9H), 3.06 (t, 4H), 3.73 (t, 4H), 4.97 (s, 2H), 6.66 (dd, 1H), 6.91 (d, 1H), 7.01-7.05 (m, 1H), 7.09-7.14 (m, 1H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07902239B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-5fbda8b809dd43cf9868a0ec889ba50f
출처 메모uspto-grants-2011_03