Reaction #1136
ord-78d0ff9eaef04c19a3803165f28b1df6
Reaction equation
pyridine
fumaric acid
amine
5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine
→
5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine fumarate
Yield 70.0%
Reagents
None
Solvents
Conditions
Detailed conditions
See reaction.notes.procedure_details.
Workup
- 1OtherAfter 30 minutes the solvent was removed in vacuo
Procedure
The above described pyridine derivative was converted into invention compound of Formula I by the addition of one equivalent of fumaric acid to a methanol (15 mL) solution of the free amine at 25° C. After 30 minutes the solvent was removed in vacuo and the residue pumped under high vacuum. Trituration with diethyl ether resulted in the formation of 5-(4-fluorophenyl)-3-(2-piperidinyl)pyridine fumarate (70%) as a colorless solid.