Sodium Hydroxide → HCID 44456288, compound
Reaction equation
[CH:1]1([CH2:7][C:8]2([CH3:37])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]([OH:18])=[C:10]([C:19]3[NH:24][C:23]4[CH:25]=[CH:26][C:27]([NH:29][S:30]([CH3:33])(=[O:32])=[O:31])=[CH:28][C:22]=4[S:21](=[O:35])(=[O:34])[N:20]=3)[C:9]2=[O:36])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.[OH-].[Na+:39]>O>[CH:1]1([CH2:7][C:8]2([CH3:37])[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[C:11]([O-:18])=[C:10]([C:19]3[NH:24][C:23]4[CH:25]=[CH:26][C:27]([NH:29][S:30]([CH3:33])(=[O:32])=[O:31])=[CH:28][C:22]=4[S:21](=[O:34])(=[O:35])[N:20]=3)[C:9]2=[O:36])[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6]1.[Na+:39]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 25 °C
Procedure
A suspension of the product of Example 41I (0.968 g) in water (5 mL) and treated with 0.997N sodium hydroxide solution (1.78 mL, 1.77 mmol) and stirred at 25° C. for 1 hour. The solution was lyophilized to give the title compound (0.602 g, 60%). 1H NMR (300 MHz, DMSO-d6): δ ppm 0.75 (m, 6H) 1.10 (m, 1H) 1.38 (m, 7H) 1.75 (m, 1H) 2.22 (m, 1H) 2.95 (m, 3H) 7.31 (m, 3H) 7.45 (m, 3H) 8.05 (m, 1H) 9.87 (m, 1H) 15.55 (m, 1H). MS (ESI−) m/z 542 (M−H)−.
Sources & evidence
- ORD record
- ord-44c6289d02854a0caa86d029e6d2972f
- Source dataset
- uspto-grants-2009_05
- Patent number
- US07538105B2
Reaction notes
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