Reaction #2201148
Related Literature (1)
openreactiondata ↗doi:10.6084/m9.figshare.5104873.v1; patent:US08816079B2
Conditions: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
Procedure: Using 5-methylisothiazolidine 1,1-dioxide (360 mg) described in Preparation Example 5 and (4-bromo-2-methanesulfonylphenyl)[4-(2,4-dimethylphenyl)piperazin-1-yl]methanone (803 mg) described in Preparation Example 110 and by the reaction and treatment in the same manner as in Example 4, the title compound (191 mg) was obtained. described in Preparation Example 110 and by the reaction and treatment in the same manner as in Example 4
Source ID: ord-5c95d9b4df97420f98e96ed8c9563c61