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HRID 383616作成日:2026年10月27日

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

https://huagongshe.com/reaction/383616

反応式

関与物質

役割名称HCID仕込み量
反応物NitrogenHCID 947—
反応物N-(3-Nitro-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamideHCID 9411047—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物N-(3-Amino-phenyl)-3-(3,4,5-trimethoxy-phenyl)-propionamideHCID 1622505499%

反応手順

(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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08367677B2
出典データセットuspto-grants-2013_02
ORD IDord-9ede8fb8e0f041c595165695f309931d
出典メモuspto-grants-2013_02