1,2-Dichloroethane → 2-Methyl-3-((S)-2-pyrrolidin-1-ylmethyl-pyrrolidine-1-carbonyl)-4,5-dihydro-1H-cyclopenta[b]pyrrol-6-one
Reaction equation
[CH3:1][C:2]1[NH:6][C:5]2[C:7](=[O:10])[CH2:8][CH2:9][C:4]=2[C:3]=1[C:11]([OH:13])=O.C1C=CC2N(O)N=NC=2C=1.C(Cl)CCl.[NH:28]1[CH2:32][CH2:31][CH2:30][C@H:29]1[CH2:33][N:34]1[CH2:38][CH2:37][CH2:36][CH2:35]1>CN(C=O)C>[CH3:1][C:2]1[NH:6][C:5]2[C:7](=[O:10])[CH2:8][CH2:9][C:4]=2[C:3]=1[C:11]([N:28]1[CH2:32][CH2:31][CH2:30][C@H:29]1[CH2:33][N:34]1[CH2:38][CH2:37][CH2:36][CH2:35]1)=[O:13]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 2-methyl-6-oxo-1,4,5,6-tetrahydro-cyclopenta[b]pyrrole-3-carboxylic acid (Example B, 3.58 g, 20 mmol), HOBt (2.7 g, 20 mmol) and EDC (5.74 g, 30 mmol) in dry DMF (50 mL) was stirred at 0° C. to room temperature for 20 min. Then (S)-(+)-1-(2-pyrrolidinylmethyl)pyrrolidine (24 mmol) was added and stirring was continued for 48 hours. The solvent was removed under reduced pressure and the residue was dissolved in EtOAc, washed with sat. Na2CO3, dried, concentrated and purified on a silica gel column to give 5.1 g (81%) of the titled compound as a yellowish foam.
Workup
- stirringstirring
- waitwas continued for 48 hours
- customThe solvent was removed under reduced pressure
- dissolutionthe residue was dissolved in EtOAc
- washwashed with sat. Na2CO3
- customdried
- concentrationconcentrated
- custompurified on a silica gel column
Sources & evidence
- ORD record
- ord-159715445ea846159869f66922c4f0fc
- Source dataset
- uspto-grants-2006_09
- Patent number
- US07105562B2
Reaction notes
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