Hydrogen chloride-ethyl acetate → HCID 70205032, compound
Reaction equation
[O:1]=[S:2]1(=[O:39])[CH2:7][CH2:6][CH2:5][N:4]2[C:8](=[O:38])[N:9]([CH2:19][CH2:20][CH2:21][NH:22][C:23](=[O:37])[CH2:24][CH2:25][CH2:26][S:27][C:28]3[N:33]4[CH:34]=[CH:35][N:36]=[C:32]4[CH:31]=[CH:30][CH:29]=3)[C:10](=[O:18])[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:3]12.[ClH:40].C(OCC)(=O)C>CO>[ClH:40].[O:39]=[S:2]1(=[O:1])[CH2:7][CH2:6][CH2:5][N:4]2[C:8](=[O:38])[N:9]([CH2:19][CH2:20][CH2:21][NH:22][C:23](=[O:37])[CH2:24][CH2:25][CH2:26][S:27][C:28]3[N:33]4[CH:34]=[CH:35][N:36]=[C:32]4[CH:31]=[CH:30][CH:29]=3)[C:10](=[O:18])[C:11]([C:12]3[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:3]12Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a methanol solution of 683 mg (1.2 mmol) of 4-(imidazo[1,2-a]pyridin-5-ylthio)butanoic [3-(1,1,6,8-tetraoxo-9-phenyl-2,3,4,8-tetrahydropyrimido[6,1-b][1,3]thiazine-7-yl)propyl]amide, 0.5 ml of 4N hydrochloric acid-ethyl acetate was added, followed by stirring. After the solvent was distilled off, the residue was washed with ether to yield 658 mg (90.7%, white crystal) of the desired product.
Workup
- distillationAfter the solvent was distilled off
- washthe residue was washed with ether
Sources & evidence
- ORD record
- ord-2731e8e7cfec4b1692e116202dabfcc6
- Source dataset
- uspto-grants-1998_11
- Patent number
- US05840732
Reaction notes
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