Lithium Hydroxide → HCID 21710833, compound
Reaction equation
[Li+].[OH-:2].COC(=O)[C@@H:6]([NH:14][C:15]([C:17]1[NH:18][C:19]2[C:24]([CH:25]=1)=[CH:23][C:22]([Cl:26])=[CH:21][CH:20]=2)=[O:16])[CH2:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C1[CH2:32][O:31]CC1>>[Cl:26][C:22]1[CH:23]=[C:24]2[C:19](=[CH:20][CH:21]=1)[NH:18][C:17]([C:15]([NH:14][C:6]1[CH:7]=[CH:8][CH:13]=[CH:12][C:11]=1[CH:10]([CH3:9])[C:32]([OH:31])=[O:2])=[O:16])=[CH:25]2Participants
4
Procedure
Aqueous 2M LiOH (33.10 ml) was added to a solution of (2S)-[(5-chloro-1H-indole-2carbonyl)-amino]-3-phenyl-propionic acid methyl ester (21.47 g, 60 mmol) in THF (140 ml) at 0-5° C. After 0.5 hour, the mixture was partially concentrated, acidified to pH 1-2 with 6N HCl, concentrated to dryness, and the solids washed with water and then ether to yield a colorless solid (18.78 g, 91%): mp 248-255° C.; HPLC (60/40) 5.21 minutes (98%); TSPMS 343/345 (MH+, 100%).
Workup
- concentrationthe mixture was partially concentrated
- concentrationconcentrated to dryness
- washthe solids washed with water
Sources & evidence
- ORD record
- ord-6596360489f246e39cdfb66e4905eb44
- Source dataset
- uspto-grants-2001_08
- Patent number
- US06277877B1
Reaction notes
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