(3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

Base Information

Chemical Name:(3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide
CAS No.:1352831-42-5
Molecular Formula:C₂₉H₂₉N₅O₄
Molecular Weight:511.58
Hs Code.:

(3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

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Chemical Property of (3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

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Technology Process of (3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

There total 4 articles about (3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 91.0%

: 63-91-2,25191-15-5,658-69-5,67675-33-6
L-phenylalanine

: C₆H₁₀N₂O₂

: 1352831-40-3
2-(4-dimethylamino-1,8-naphthalimido)ethyl isocyanide

: 1352831-42-5
(3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

Guidance literature:: In 2,2,2-trifluoroethanol; at 20 ℃; for 3h;
DOI:10.1002/chem.201102096

Reference yield:

: 81-84-5
1,8-Naphthalic anhydride

: 1352831-42-5
(3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

Guidance literature:: Multi-step reaction with 4 steps

1.1: bromine; potassium hydroxide / water / 18 h / 0 - 60 °C

1.2: 20 °C / Reflux

2.1: ethanol / 0.5 h / Reflux

3.1: triethylamine; trichlorophosphate / dichloromethane / 20 °C / Cooling with ice

4.1: 2,2,2-trifluoroethanol / 3 h / 20 °C

With bromine; triethylamine; potassium hydroxide; trichlorophosphate; In ethanol; dichloromethane; 2,2,2-trifluoroethanol; water;
DOI:10.1002/chem.201102096

Reference yield:

: 1352831-39-0
2-(4-dimethylamino-1,8-naphthalimido)ethylformamide

: 1352831-42-5
(3S,5R,6S)-3-benzyl-N-(2-(6-(dimethylamino)-1,3-dioxo-1H-benzo[de]isoquinolin-2(3H)-yl)ethyl)-2-oxo-1,4-diazabicyclo[4.1.0]heptane-5-carboxamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine; trichlorophosphate / dichloromethane / 20 °C / Cooling with ice

2: 2,2,2-trifluoroethanol / 3 h / 20 °C

With triethylamine; trichlorophosphate; In dichloromethane; 2,2,2-trifluoroethanol;
DOI:10.1002/chem.201102096