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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 507292생성일: 2026년 10월 26일

Potassium Carbonate → (2R)-2-[N-(4-Chlorobenzenesulfonyl)-N-(4-methoxybenzyl)amino]-4-methylpentanoic acid amide

https://huagongshe.com/reaction/507292

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물4-Methyloxybenzyl chlorideHCID 69993—
반응물(2R)-2-(4-Chlorobenzenesulfonylamino)-4-methylpentanoic acid amideHCID 59001058—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물(2R)-2-[N-(4-Chlorobenzenesulfonyl)-N-(4-methoxybenzyl)amino]-4-methylpentanoic acid amideHCID 986706770%

반응 단계

(2R)-2-(4-Chlorobenzenesulfonylamino)-4-methylpentanoic acid amide (300 mg, 1 mmol), K2CO3 (170 mg, 1.2 mmol), and 4-methoxybenzyl chloride (170 mg, 1.1 mmol) in DMF (25 mL) was heated to 60° C. for 18 h. The reaction was then diluted with EtOAc (150 mL) and washed with H2O, brine, dried over MgSO4 and concentrated to give a crude white wax. Further purification by flash chromatography (SiO2, 25% EtOAc/hexanes) afforded the titled compound (297 mg) as a white solid in 70% yield. [α]D=+44.2 (c 1.00, MeOH); MS (ESI), (M−H)− 422.9; 1H NMR (CDCl3) δ 7.63 (d, 2H, J=7.0), 7.42 (d, 2H, J=7.0), 7.25 (d, 2H, J=8.0), 6.79 (d, 2H, J=8.0), 6.25 (br s, 1H), 5.35 (br s, 1H), 4.36 (dd, 2H, J=50, 15), 4-26 (t, 1H, J=7.2), 3.78 (s, 3H), 1.83 (m, 1H), 1.18-1.34 (m, 2H), 0.75 (d, 3H, J=7.0), 0.67 (d, 3H, J=7.0); IR (KBr) 3480, 2959, 1693, 1674, 1514, 1333, 1158 cm−1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07786122B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-fb240e896cc6475fac058c58c89c2da3
출처 메모uspto-grants-2010_08