HCID 68452390, compound → HCID 68454615, compound
Reaction equation
[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([NH:15][CH:16]1[CH2:20][CH2:19][N:18](CC3C=CC=CC=3)[CH2:17]1)=[CH:10][CH:9]=2)=[O:5])[CH3:2]>C(O)C.C(O)(=O)C.[Pd]>[CH2:1]([O:3][C:4]([C:6]1[NH:7][C:8]2[C:13]([CH:14]=1)=[CH:12][C:11]([NH:15][CH:16]1[CH2:20][CH2:19][NH:18][CH2:17]1)=[CH:10][CH:9]=2)=[O:5])[CH3:2]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
A solution of 2.8 g (7 mmol) 5-(1-benzyl-pyrrolidin-3-ylamino)-1H-indole-2-carboxylic acid ethyl ester in 180 ml ethanol and 20 ml acetic acid was hydrogenated over Pd/C for 24 h at room temperature. After filtration and evaporation the residue was taken up in 200 ml 10% NaHCO3 aq. and extracted with 150 ml dichloromethane (DCM). The aqueous phase was washed 7 times with 80 ml DCM each and the combined organic phases were dried over Na2SO4. After filtration and evaporation to dryness the residue was purified over Isolute® SPE (solid phase extraction) eluting with a gradient formed from DCM/2N NH3 in methanol to yield 1.05 g (74%) of the title compound and light brown crystals. MS (m/e): 274.3 (MH+, 100%).
Workup
- filtrationAfter filtration and evaporation the residue
- extractionextracted with 150 ml dichloromethane (DCM)
- washThe aqueous phase was washed 7 times with 80 ml DCM each and the combined organic phases
- dry with materialwere dried over Na2SO4
- filtrationAfter filtration and evaporation to dryness the residue
- customwas purified over Isolute® SPE (solid phase extraction)
- washeluting with a gradient
- customformed from DCM/2N NH3 in methanol
Sources & evidence
- ORD record
- ord-83080f4809b846c3b75bb48827067524
- Source dataset
- uspto-grants-2010_07
- Patent number
- US07754736B2
Reaction notes
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