Lithium Hydroxide → HCID 67074652, compound
Reaction equation
[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C:19]([C:22]([O:24]C)=[O:23])([CH3:21])[CH3:20])[C:13](=[O:26])[C@@H:12]1[CH3:27])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[OH-].[Li+]>>[CH2:1]([O:8][C:9]([N:11]1[CH2:16][CH2:15][N:14]([CH2:17][CH2:18][C:19]([C:22]([OH:24])=[O:23])([CH3:20])[CH3:21])[C:13](=[O:26])[C@@H:12]1[CH3:27])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
3
Procedure
In analogy to the procedure described in Example 23B, (S)-4-(3-methoxycarbonyl-3-methyl-butyl)-2-methyl-3-oxo-piperazine-1-carboxylic acid benzyl ester and 1 M aq. lithium hydroxide solution gave the titled compound in 70% yield as light yellow oil. MS: 363.19 (MH+).
Sources & evidence
- ORD record
- ord-ffec92b7dbfd4ae1b95a2d6adfc3a656
- Source dataset
- uspto-grants-2013_05
- Patent number
- US08445674B2
Reaction notes
Loading…