HCID 58236597, compound → HCID 58236599, compound
Reaction equation
[C:1]([O:5][C:6]([N:8]([CH2:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]2[S:28][C:27]3[C:22](=[N:23][CH:24]=[CH:25][C:26]=3[O:29][C:30]3[CH:35]=[CH:34][C:33]([NH:36][C:37](=[O:43])[CH2:38][C:39]([O:41]C)=[O:40])=[CH:32][C:31]=3[F:44])[CH:21]=2)=[N:18][CH:19]=1)[CH2:9][CH2:10][O:11][CH3:12])=[O:7])([CH3:4])([CH3:3])[CH3:2]>C1COCC1.O>[C:1]([O:5][C:6]([N:8]([CH2:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]2[S:28][C:27]3[C:22](=[N:23][CH:24]=[CH:25][C:26]=3[O:29][C:30]3[CH:35]=[CH:34][C:33]([NH:36][C:37](=[O:43])[CH2:38][C:39]([OH:41])=[O:40])=[CH:32][C:31]=3[F:44])[CH:21]=2)=[N:18][CH:19]=1)[CH2:9][CH2:10][O:11][CH3:12])=[O:7])([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
To a solution of compound 342 (540 mg, 0.864 mmol) in THF (12 ml) and water (6 ml) was added LiOH monohydrate (363 mg, 8.64 mmol). The mixture was stirred 48 h at room temperature and THF was removed under reduced pressure. The aqueous solution was diluted with water (10 ml) and acidified to pH 4 using 1N HCl. The suspension was filtered and the precipitate was dried under high vacuum to afford compound 343 (485 mg, 0.79 mmol, 92% yield) as a beige solid. MS (m/z): 611.5 (M+H).
Workup
- customTHF was removed under reduced pressure
- additionThe aqueous solution was diluted with water (10 ml)
- filtrationThe suspension was filtered
- customthe precipitate was dried under high vacuum
Sources & evidence
- ORD record
- ord-fd1e37aaf47c4ded80283b5069c94d98
- Source dataset
- uspto-grants-2014_06
- Patent number
- US08759522B2
Reaction notes
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