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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 343195생성일: 2026년 10월 25일

O-Phenylenediamine → 2-[3-(2-Amino-phenylcarbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl]-N-isopropyl-N-phenyl acetamide

https://huagongshe.com/reaction/343195

반응식

참여 물질

역할이름HCID투입량
반응물O-PhenylenediamineHCID 7243—
반응물DiisopropylethylamineHCID 81531—
반응물PyBroPHCID 2733179—
반응물[1-(isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]acetic acidHCID 67696769—
반응물{3-(Benzyloxycarbonyl-methyl)-1-[isopropyl-(4-methoxy-phenyl)-carbamoylmethyl]-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl}acetic acidHCID 86753587—
용매DimethylformamideHCID 6228—
생성물2-[3-(2-Amino-phenylcarbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl]-N-isopropyl-N-phenyl acetamideHCID 67697296—

반응 조건

온도50 °C

반응 단계

A stirring solution of 100 mg (0.20 mmol) of [1-(Isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]-acetic acid, prepared as in Intermediate 7, 32 mg (0.30 mmol, 1.5 equiv) of 1,2-phenylene diamine, 187 mg (0.40 mmol, 2.0 equiv) of bromo-tris-pyrrolidino-phosphonium hexafluorophosphate (PyBroP), and 80 mg (0.60 mmol, 3.0 equiv) of diisopropylethylamine in 2 mL of DMF is heated at 50° C. for 48 h. The DMF is removed in vacuo and the residue is dissolved in 20 mL of EtOAc and extracted with 20 mL 1N HCl. The organic layer is dried (MgSO4) and the solvent removed in vacuo. The resulting oil is purified by silica gel flash column chromatography using dichloromethane/MeOH 20/1 as eluent followed by further purification via reverse phase MPLC using a C-18 column and 60% acetonitrile/40% H2O with 0.1% TFA as eluent followed by lyophilization to afford 30 mg of the title compound as a white amorphous solid: 1H NMR (CDCl3, 300 MHz) δ9.38 (s, 0.7H), 9.17 (s, 0.3H), 7.53-7.04 (m, 17H), 6.81 (d, 1H, J=4.7), 4.97 (m, 1H), 4.57 (d, 0.5H, J=16.6), 4.27 (s, br, 2H), 3.87 (d, 0.5H, J=16.6), 3.36 (d, 1H, J=15.6), 3.13 (d, 1H, J=15.6), 2.60 (d, 0.5H, J=15.3), 2.42 (d, 0.5H, J=15.3), 1.61 (s, 1H), 1.22 (s, 2H), 1.09 (m, 6H); low resolution MS (FAB)m/e 590 (MH+), 482.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05859007
출처 데이터셋uspto-grants-1999_01
ORD IDord-a22dfe043c31444e85885ce42874c5b0
출처 메모uspto-grants-1999_01