Water → HCID 136052270, compound
Reaction equation
[CH2:1]([C:3]1[S:40][C:6]2[N:7]([CH2:21][C:22]3[CH:27]=[CH:26][C:25]([C:28]4[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=4[C:34]4[NH:38][C:37](=[O:39])[O:36][N:35]=4)=[CH:24][CH:23]=3)[C:8](=[O:20])[N:9]([CH2:12][C:13](=[O:19])[C:14]([CH3:18])([CH3:17])[CH2:15][OH:16])[C:10](=[O:11])[C:5]=2[CH:4]=1)[CH3:2].[C:41](OC(=O)C)(=[O:43])[CH3:42].C(OCC)(=O)C.O>N1C=CC=CC=1>[C:41]([O:16][CH2:15][C:14]([CH3:18])([CH3:17])[C:13](=[O:19])[CH2:12][N:9]1[C:10](=[O:11])[C:5]2[CH:4]=[C:3]([CH2:1][CH3:2])[S:40][C:6]=2[N:7]([CH2:21][C:22]2[CH:27]=[CH:26][C:25]([C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[C:34]3[NH:38][C:37](=[O:39])[O:36][N:35]=3)=[CH:24][CH:23]=2)[C:8]1=[O:20])(=[O:43])[CH3:42]Participants
6
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 6-ethyl-3-(4-hydroxy-3,3-dimethyl-2-oxobutyl)-1-{[2′-(5-oxo-4,5-dihydro-1,2,4-oxadiazol-3-yl)biphenyl-4-yl]methyl}thieno[2,3-d]pyrimidine-2,4(1H,3H)-dione (0.1 g) in pyridine (0.5 mL) was added acetic anhydride (0.034 mL), and the mixture was stirred at room temperature for 15 hr. To the reaction mixture were added ethyl acetate and water, and the mixture was extracted with ethyl acetate.
Workup
- extractionthe mixture was extracted with ethyl acetate
Sources & evidence
- ORD record
- ord-fe4c318bfcb147b39a70005a051e3a5e
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08501750B2
Reaction notes
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