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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 383616생성일: 2026년 10월 26일

Nitrogen → N-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamide

https://huagongshe.com/reaction/383616

반응식

참여 물질

역할이름HCID투입량
반응물NitrogenHCID 947—
반응물N-(3-Nitro-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamideHCID 9411047—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
생성물N-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamideHCID 1622505499%

반응 단계

(The following reaction is done in an N2 atmosphere.) Dissolve N-(3-Nitro-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamide (89) (100 mg, 0.28 mmol) in MeOH (4.5 mL) and add Pd on carbon (10% (w/w) Pd content, 29.5 mg, 0.028 mmol) followed by NH4CO2H (175 mg, 2.77 mmol) at rt. Degas the reaction mixture carefully (flush with N2) and stir it for 75 min at rt. Filtrate reaction mixture through a short pad of celite and remove solvent. Treat residue with EtOAc, filtrate again through a short pad of celite and remove solvent to obtain N-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamide (90) (91 mg, 99%) as a white solid. No further purification. 1H NMR (400 MHz, CD3OD): 2.65 (t, 2H, J=7.5 Hz); 2.98 (t, 2H, J=7.5 Hz); 3.75 (s, 3H); 3.82 (s, 6H); 6.50 (dd, 1H, J1=8.0 Hz, J2=2.0 Hz); 6.58 (s, 2H); 6.80 (dd, 1H, J=8.0 Hz, J2=2.0 Hz); 7.02-7.07 (m, 1H); 7.04 (t, 1H, J=8.0 Hz).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08367677B2
출처 데이터셋uspto-grants-2013_02
ORD IDord-9ede8fb8e0f041c595165695f309931d
출처 메모uspto-grants-2013_02