5-Chloro-1H-indole-2-carboxylic acid → HCID 54395516, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:14])[C:4]([NH2:13])([CH3:12])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1.[Cl:15][C:16]1[CH:17]=[C:18]2[C:22](=[CH:23][CH:24]=1)[NH:21][C:20]([C:25](O)=[O:26])=[CH:19]2>ClCCl.CN(C)C=O>[CH3:1][O:2][C:3](=[O:14])[C:4]([NH:13][C:25]([C:20]1[NH:21][C:22]2[C:18]([CH:19]=1)=[CH:17][C:16]([Cl:15])=[CH:24][CH:23]=2)=[O:26])([CH3:12])[CH2:5][C:6]1[CH:11]=[CH:10][CH:9]=[CH:8][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Racemic 2-amino-2-methyl-3-phenyl-propionic acid methyl ester (200 mg, 0.87 mmol) and 5-chloro-1H-indole-2-carboxylic acid (170 mg, 0.87 mmol) were coupled according to Procedure A (2:1 dichloromethane/dimethylformamide solvent) and the product purified by chromatography on silica gel eluted with 10% ethyl acetate in hexanes. Yield 286 mg, 89%; HPLC (60/40) 9.63 minutes (85%); TSPMS 371/373 (MH+, 100%);
Workup
- customthe product purified by chromatography on silica gel
- washeluted with 10% ethyl acetate in hexanes
- customHPLC (60/40) 9.63 minutes (85%)
Sources & evidence
- ORD record
- ord-b17010129274420598f363b5ebc9ef8b
- Source dataset
- uspto-grants-2000_08
- Patent number
- US06107329
Reaction notes
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