tert-Butoxy bis(dimethylamino)methane → 4-(3-Dimethylamino-2-methoxymethyl-acryloyl)-1H-pyrrole-2-carboxylic Acid (2-hydroxy-1-(S)-phenyl-ethyl)-amide
Reaction equation
[OH:1][CH2:2][C@@H:3]([NH:10][C:11]([C:13]1[NH:14][CH:15]=[C:16]([C:18](=[O:23])[CH2:19][CH2:20][O:21][CH3:22])[CH:17]=1)=[O:12])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.CC(O[CH:29](N(C)C)[N:30]([CH3:32])[CH3:31])(C)C>C1COCC1>[OH:1][CH2:2][C@@H:3]([NH:10][C:11]([C:13]1[NH:14][CH:15]=[C:16]([C:18](=[O:23])[C:19]([CH2:20][O:21][CH3:22])=[CH:29][N:30]([CH3:32])[CH3:31])[CH:17]=1)=[O:12])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
4-(3-Methoxy-propionyl)-1H-pyrrole-2-carboxylic acid (2-hydroxy-1-(S)-phenyl-ethyl)-amide was treated with an excess of Bredereck's reagent in THF at room temperature to 50° C. for 3 days. The solvent was removed under reduced pressure and the concentrate was used directly in the next step. HPLC Method B, Rt=5.0 minutes “broad peak”.
Workup
- customThe solvent was removed under reduced pressure
Sources & evidence
- ORD record
- ord-e46794f0307549989947e9e6ad03485a
- Source dataset
- uspto-grants-2008_03
- Patent number
- US07345054B2
Reaction notes
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