Lithium Hydroxide → HCID 68675578, compound
Reaction equation
[Li+].[OH-].[CH2:3]([O:10][C:11]1[C:43]([CH3:44])=[CH:42][C:14]([CH2:15][C@@H:16]([CH2:21][C:22](=[O:41])[N:23]2[CH2:28][CH2:27][CH:26]([N:29]3[CH2:35][CH2:34][C:33]4[CH:36]=[CH:37][CH:38]=[CH:39][C:32]=4[NH:31][C:30]3=[O:40])[CH2:25][CH2:24]2)[C:17]([O:19]C)=[O:18])=[CH:13][C:12]=1[CH3:45])[C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1>O.C1COCC1>[CH2:3]([O:10][C:11]1[C:43]([CH3:44])=[CH:42][C:14]([CH2:15][C@@H:16]([CH2:21][C:22](=[O:41])[N:23]2[CH2:28][CH2:27][CH:26]([N:29]3[CH2:35][CH2:34][C:33]4[CH:36]=[CH:37][CH:38]=[CH:39][C:32]=4[NH:31][C:30]3=[O:40])[CH2:25][CH2:24]2)[C:17]([OH:19])=[O:18])=[CH:13][C:12]=1[CH3:45])[C:4]1[CH:5]=[CH:6][CH:7]=[CH:8][CH:9]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 200 mg (8.35 mmol) LiOH in 40 mL water was added to a solution of 2.43 g (4.16 mmol) methyl (S)-2-(4-benzyloxy-3,5-dimethyl-benzyl)-4-oxo-4-[4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidin-1-yl]-butanoate in 80 mL THF and the reaction mixture was stirred for 1 h at RT. The mixture was evaporated down i.vac., the residue was taken up in 100 mL water and acidified with 2 M HCl with stirring. The precipitate formed was separated off and dried at 40° C.
Workup
- customThe mixture was evaporated down i.vac
- stirringwith stirring
- customThe precipitate formed
- customwas separated off
- customdried at 40° C.
Sources & evidence
- ORD record
- ord-9a413b994a654b6994c541054416e559
- Source dataset
- uspto-grants-2010_04
- Patent number
- US07696209B2
Reaction notes
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