Ammonium formate → HCID 23292348, compound
Reaction equation
C([O-])=O.[NH4+].[NH2:5][CH2:6][CH:7]([N:20](CC1C=CC=CC=1)[C@@H](C1C=CC=CC=1)C)[CH2:8][CH:9]1[CH2:18][CH2:17][C:16]2[C:11](=[CH:12][C:13]([F:19])=[CH:14][CH:15]=2)[CH2:10]1>CO.[Pd]>[F:19][C:13]1[CH:12]=[C:11]2[C:16]([CH2:17][CH2:18][CH:9]([CH2:8][CH:7]([NH2:20])[CH2:6][NH2:5])[CH2:10]2)=[CH:15][CH:14]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
0.45 g of ammonium formate is added to a vigorously stirred suspension of 0.35 g (0.84 mmol) of the compound obtained in Step 4 and 0.25 g of Pd/C 10% in 25 ml of CH3OH. After stirring for 1 hour under reflux, the mixture is cooled and filtered; the catalyst is washed with CH3OH and the combined filtrates are concentrated in vacuo to yield the title compound in the form of an oil, which is used without purification in the following reaction.
Workup
- temperatureunder reflux
- temperaturethe mixture is cooled
- filtrationfiltered
- washthe catalyst is washed with CH3OH
- concentrationthe combined filtrates are concentrated in vacuo
Sources & evidence
- ORD record
- ord-03888e07dc034d0daa3c4f3e64a01128
- Source dataset
- uspto-grants-2000_10
- Patent number
- US06127396
Reaction notes
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