Lithium Hydroxide → HCID 67273559, compound
Reaction equation
[Li+].[OH-:2].[O:3]=[C:4]1[N:10]([CH:11]2[CH2:16][CH2:15][N:14]([C:17]([O:19][C@@H:20](OC)[C:21](=C=O)[C:22]3[CH:27]=[C:26]([CH3:28])[C:25]([O:29][CH2:30][C:31]4[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=4)=[C:24]([CH2:37][CH3:38])[CH:23]=3)=[O:18])[CH2:13][CH2:12]2)[CH2:9][CH2:8][C:7]2[CH:43]=[CH:44][CH:45]=[CH:46][C:6]=2[NH:5]1.C1[CH2:51][O:50]CC1>O>[O:3]=[C:4]1[N:10]([CH:11]2[CH2:16][CH2:15][N:14]([C:17]([O:19][C@@H:20]([C:51]([OH:50])=[O:2])[CH2:21][C:22]3[CH:27]=[C:26]([CH3:28])[C:25]([O:29][CH2:30][C:31]4[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=4)=[C:24]([CH2:37][CH3:38])[CH:23]=3)=[O:18])[CH2:13][CH2:12]2)[CH2:9][CH2:8][C:7]2[CH:43]=[CH:44][CH:45]=[CH:46][C:6]=2[NH:5]1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 50 mg (2.09 mmol) LiOH in 5 mL water was added to a solution of 800 mg (1.33 mmol) (R)-2-(4-benzyloxy-3-ethyl-5-methyl-phenyl)-1-methoxy-carbonyl-ethyl 4-(2-oxo-1,2,4,5-tetrahydro-1,3-benzodiazepin-3-yl)-piperidine-1-carboxylate in 15 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 50 mL water, and 2 M HCl was added until an acidic reaction was obtained. The precipitate formed was filtered off, washed with water and dried. Further purification was carried out by decocting with 150 mL water, filtration and drying again.
Workup
- customThe mixture was evaporated down i.vac
- addition2 M HCl was added until an acidic reaction
- customwas obtained
- customThe precipitate formed
- filtrationwas filtered off
- washwashed with water
- customdried
- customFurther purification
- filtrationby decocting with 150 mL water, filtration
- customdrying again
Sources & evidence
- ORD record
- ord-5f9b4a0152184334b4dc756075bd540d
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582625B2
Reaction notes
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