Lithium hydroxide, monohydrate → HCID 23121814, compound
Reaction equation
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:31]=[C:32]([O:34][CH2:35][C:36]2[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=2)[CH:33]=1)[C:12]([NH:14][C:15]1[N:20]=[CH:19][C:18]([NH:21][C:22](=[O:30])[C:23]([O:26]C(=O)C)([CH3:25])[CH3:24])=[CH:17][CH:16]=1)=[O:13])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.O[Li].O>CO.O.C1COCC1>[CH2:35]([O:34][C:32]1[CH:31]=[C:11]([CH:10]=[C:9]([O:8][CH2:1][C:2]2[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=2)[CH:33]=1)[C:12]([NH:14][C:15]1[N:20]=[CH:19][C:18]([NH:21][C:22](=[O:30])[C:23]([OH:26])([CH3:25])[CH3:24])=[CH:17][CH:16]=1)=[O:13])[C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1Participants
6
Reactant 2
Product 1
Reagents, catalysts & solvents 3
Procedure
To a stirred suspension of N-{6-[(3,5-dibenzyloxybenzoyl)amino]-pyridin-3-yl}-2-acetoxy-2-methyl-propionamide (158 mg) in methanol (10 ml) was added a solution of LiOH.H2O (30 mg) in water (1 ml) and THF (3 ml). The mixture was stirred at ambient temperature for 20 hours. Volatile material was removed by evaporation. To the residue was added water (10 ml). Made acidic with 2M hydrochloric acid. Precipitate filtered off, washed with ethyl acetate, and dried under high vacuum to give the title compound (120 mg) as a solid, 1H NMR δ d6-DMSO): 1.35 (s, 6H), 5.18 (s, 4H), 6.88 (s, 1H), 7.28 to 7.48 (m, 12H), 8.08 (d, 1H), 8.22 (d, 1H), 8.82 (s, 1H), 9.90 (s, 1H), 10.96 (s, 1H). MS ES+ 512.16 (M+H)+.
Workup
- customVolatile material was removed by evaporation
- additionTo the residue was added water (10 ml)
- filtrationPrecipitate filtered off
- washwashed with ethyl acetate
- customdried under high vacuum
Sources & evidence
- ORD record
- ord-48b3f9344f78465e9ed86ac56b5ca473
- Source dataset
- uspto-grants-2011_05
- Patent number
- US07951830B2
Reaction notes
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