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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1893848생성일: 2026년 10월 26일

Cesium carbonate → (2R)-2-[N-(4-Allyloxy-3-fluorobenzyl)-N-(4-chlorobenzenesulfonyl)amino]-4-methyl-pentanoic acid amide

https://huagongshe.com/reaction/1893848

반응식

참여 물질

역할이름HCID투입량
반응물Cesium carbonateHCID 10796—
반응물(2R)-2-(4-Chlorobenzenesulfonylamino)-4-methylpentanoic acid amideHCID 59001058—
반응물1-Allyloxy-4-bromomethyl-2-fluorobenzeneHCID 67198367—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(2R)-2-[N-(4-Allyloxy-3-fluorobenzyl)-N-(4-chlorobenzenesulfonyl)amino]-4-methyl-pentanoic acid amideHCID 1015185326%

반응 단계

To a solution of (2R)-2-(4-chlorobenzenesulfonylamino)-4-methyl-pentanoic acid amide (1.00 g, 3.29 mmol), and Cs2CO3 (1.29 g, 3.95 mmol) in DMF (25 mL) was added 1-allyloxy-4-bromomethyl-2-fluorobenzene (ref.: Graham, S. L. et al., EP Patent Application No. EP 487270 (1992): 0.88 g, 3.67 mmol). The resulting solution was stirred at rt for 18 h. The reaction was then diluted with 9:1 EtOAc:hexanes (350 mL) and washed with H2O (4×200 mL), brine, and dried over Na2SO4, to afford the titled compound (393 mg) as a white solid in 26% yield. MS (ESI), (M+H)+469.1; 1H NMR (CDCl3) δ 7.66 (d, 2H, J=8.1), 7.45 (d, 2H, J=8.1), 7.11 (d, 1H, J=12.0), 6.98 (m, 1H), 6.84 (t, 1H, J=8.0), 6.22 (br s, 1H), 6.04 (m, 2H), 5.42 (m, 1H), 5.16 (br s, 1H), 4.59 (m, 2H), 4.40 (m, 3H), 1.83 (m, 1H), 1.32 (m, 1H), 1.14 (m, 1H), 0.76 (d, 3H, J=7.0), 0.68 (d, 3H, J=7.0).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08513253B2
출처 데이터셋uspto-grants-2013_08
ORD IDord-c2c1422fc4094ddbb0031b9adfef3847
출처 메모uspto-grants-2013_08