Reaction #83512
ord-d1013166a27f4d7d9d1419f8148dcd43
Reaction equation
Reactants
Reagents
None
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1OtherThe methanol is evaporated
- 2workup.ADDITIONthe residue diluted with water
- 3WashThe resulting solid is washed witch water
- 4workup.DISSOLUTIONdissolved in ethyl acetate
- 5Washthe organic layer washed with saturated NaHCO3, brine
- 6Dryingdried with Na2SO4
- 7FiltrationThe mixture is filtered
- 8Otherthe filtrate evaporated in vacuo
- 9Otherto give a residue which
Procedure
A partial solution of ?? g of α-chloro-N-[4-(5H-pyrrolo[2,1-c][1,4]benzodiazepin-10(11H)-ylcarbonyl)phenyl]benzeneacetamide in 1 ml of methanol is treated with 0.5 ml of dimethylamine and 1 ml of 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone and stirring continued for 20 hours. The methanol is evaporated and the residue diluted with water. The resulting solid is washed witch water, dissolved in ethyl acetate and the organic layer washed with saturated NaHCO3, brine and dried with Na2SO4. The mixture is filtered and the filtrate evaporated in vacuo to give a residue which is stirred with ethyl acetate-hexane to give 0.15 g of a beige solid. MS(CI): 465(M+H).