Ammonia → 2-Amino-2-oxoethyl 4-{6-[3-(trifluoromethyl)phenyl]-3-pyridyl}-1-piperazinecarboxylate
Reaction equation
[NH3:1].[F:2][C:3]([F:32])([F:31])[C:4]1[CH:5]=[C:6]([C:10]2[N:15]=[CH:14][C:13]([N:16]3[CH2:21][CH2:20][N:19]([C:22]([O:24][CH2:25][C:26](OCC)=[O:27])=[O:23])[CH2:18][CH2:17]3)=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1.O1CCCC1>CO>[F:2][C:3]([F:31])([F:32])[C:4]1[CH:5]=[C:6]([C:10]2[N:15]=[CH:14][C:13]([N:16]3[CH2:21][CH2:20][N:19]([C:22]([O:24][CH2:25][C:26]([NH2:1])=[O:27])=[O:23])[CH2:18][CH2:17]3)=[CH:12][CH:11]=2)[CH:7]=[CH:8][CH:9]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5.90 ml (41.40 mmol) of a solution of ammonia (7N) in methanol are added to a solution of 0.30 g (0.69 mmol) of 2-(ethyloxy)-2-oxoethyl 4-{6-[3-(trifluoromethyl)phenyl]-3-pyridyl}-1-piperazinecarboxylate, obtained in step 7.5. of Example 7, in 6 ml of a 1/1 mixture of methanol and tetrahydrofuran. Stirring is continued at room temperature for 22 hours. After concentrating under reduced pressure, the residue obtained is purified by chromatography on silica gel, eluting with a 96/4 mixture of dichloromethane and methanol, followed by washing with diisopropyl ether. 0.19 g of pure product is obtained in the form of a yellow solid.
Workup
- customobtained in step 7.5
- concentrationAfter concentrating under reduced pressure
- customthe residue obtained
- customis purified by chromatography on silica gel
- washeluting with a 96/4 mixture of dichloromethane and methanol
- washby washing with diisopropyl ether
Sources & evidence
- ORD record
- ord-58a8fa7378cd47abb6f00fd6af0a47fa
- Source dataset
- uspto-grants-2010_03
- Patent number
- US07687503B2
Reaction notes
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