Ethanol → HCID 68896800, compound
Reaction equation
[O:1]=[S:2]1(=[O:33])[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[C:8]1[N:17]=[C:16]([C:18]([NH:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[S:28]([CH3:31])(=[O:30])=[O:29])=[O:19])[C:15]([OH:32])=[C:14]2[C:9]=1[CH:10]=[CH:11][CH:12]=[N:13]2.C(O)C.[OH-].[Na+:38]>CC(C)=O>[O:33]=[S:2]1(=[O:1])[CH2:7][CH2:6][CH2:5][CH2:4][N:3]1[C:8]1[N:17]=[C:16]([C:18]([NH:20][CH2:21][C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][C:23]=2[S:28]([CH3:31])(=[O:30])=[O:29])=[O:19])[C:15]([O-:32])=[C:14]2[C:9]=1[CH:10]=[CH:11][CH:12]=[N:13]2.[Na+:38]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
5-(1,1-dioxido-1,2-thiazinan-2-yl)-8-hydroxy-N-[2-(methylsulfonyl)benzyl]-1,6-naphthyridine-7-carboxamide (53 mg, 0.108 mmol) was suspended in a 1:1 mixture of ethanol and acetone (1 mL each). NaOH (130 uL, 1 M) was added and the starting material dissolved. After 1 hour the sodium salt precipitated. The sample was concentrated in vacuo to afford the desired material as a yellow solid.
Workup
- dissolutionthe starting material dissolved
- customAfter 1 hour the sodium salt precipitated
- concentrationThe sample was concentrated in vacuo
Sources & evidence
- ORD record
- ord-ba3ce39d8c3c495f988437b993b6fd8e
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06921759B2
Reaction notes
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