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1003316-11-7

N-[3-[[4-[(1,3-Dihydro-1,3-dioxo-2H-isoindol-2-yl)methyl]benzoyl]amino][1,1'-biphenyl]-4-yl]carbamic Acid tert-Butyl Ester synthesis

8synthesis methods
-

Yield:-

Reaction Conditions:

with potassium iodide in N,N-dimethyl-formamide at 50;

Steps:



1 , 1 -dimethyl ethyl [3-( { [4-(chloromethyl)phenyl] carbonyl}amino)biphenyl-4-yl]carbamate (20 g, 45.8 mmol), potassium phthalimide (9.33 g, 50.4 mmol) and potassium iodide (1.52 g, 9.15 mmol) were stirred in DMF (81 mL) at 50 0C overnight. Room temperature was attained, H2O was added and the products extracted into EtOAc (x2). The combined organic extracts were washed with brine, dried over MgSO4 and concentrated in vacuo. The residue was triturated in MeOH to give 1,1-dimethylethyl {3-[({4- [( 1 ,3-dioxo- 1 ,3-dihydro-2H-isoindol-2-yl)methyl]phenyl} carbonyl)amino]biphenyl-4- yl} carbamate as a pale yellow solid.

References:

WO2008/10985,2008,A2 Location in patent:Page/Page column 166-167