Ethyl Acetate → HCID 22257954, compound
Reaction equation
Cl[C:2]1[CH:3]=[C:4]([CH:9]=C[CH:11]=1)[C:5](OO)=[O:6].[OH:12][C:13]1[CH:14]=[C:15]([S:19]([C:21]2[C:29]3[C:28](=[O:30])[N:27]([CH3:31])[C:26](=[O:32])[N:25]([CH2:33][CH:34]([CH3:36])[CH3:35])[C:24]=3[S:23][C:22]=2[CH2:37][C:38]2[C:47]3[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=3)[CH:41]=[CH:40][CH:39]=2)=[O:20])[CH:16]=[CH:17][CH:18]=1.C(OCC)(=O)C>ClCCl>[CH3:11][CH2:2][CH2:3][CH:4]([CH3:9])[CH3:5].[OH:12][C:13]1[CH:14]=[C:15]([S:19]([C:21]2[C:29]3[C:28](=[O:30])[N:27]([CH3:31])[C:26](=[O:32])[N:25]([CH2:33][CH:34]([CH3:35])[CH3:36])[C:24]=3[S:23][C:22]=2[CH2:37][C:38]2[C:47]3[C:42](=[CH:43][CH:44]=[CH:45][CH:46]=3)[CH:41]=[CH:40][CH:39]=2)(=[O:6])=[O:20])[CH:16]=[CH:17][CH:18]=1Participants
6
Reactant 3
Product 2
Reagents, catalysts & solvents 1
Procedure
3-Chloroperoxybenzoic acid (50 mg) was added to a solution of 5-[(3-hydroxyphenyl)sulfinyl]-3-methyl-1-(2-methylpropyl)-6-(1-naphthalenylmethyl)thieno[2,3-d]pyrimidine-2,4-(1H,3H)-dione (Example 28, 80 mg) in dichloromethane (2 ml). After 2 hours, ethyl acetate (25 ml) was added and the solution was washed with saturated sodium bisulfite solution (10 ml), then with saturated sodium hydrogen carbonate solution (10 ml), then with brine (10 ml). The organic layer was dried over anhydrous magnesium sulfate, filtered and evaporated under reduced pressure. The residue was recrystallised from ethyl acetate:isohexane to give the title compound (24 mg).
Workup
- washthe solution was washed with saturated sodium bisulfite solution (10 ml)
- dry with materialThe organic layer was dried over anhydrous magnesium sulfate
- filtrationfiltered
- customevaporated under reduced pressure
- customThe residue was recrystallised from ethyl acetate
Sources & evidence
- ORD record
- ord-9d1e6958c0e94ca88f481b79504879da
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06984644B2
Reaction notes
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