Hydrochloric Acid → HCID 131728528, compound
Reaction equation
S(=O)(=O)(O)O.[Cl:6][C:7]1[C:12]2[O:13][C:14]3[C:23]([CH3:24])=[CH:22][C:21]([C:25]([OH:27])=[O:26])=[CH:20][C:15]=3[S:16](=[O:19])(=[O:18])[CH2:17][C:11]=2[CH:10]=[C:9]([N:28]2[CH2:33][CH2:32][NH:31][CH2:30][CH2:29]2)[CH:8]=1.Cl.[CH:35](O)([CH3:37])[CH3:36]>>[ClH:6].[CH:35]([O:26][C:25]([C:21]1[CH:22]=[C:23]([CH3:24])[C:14]2[O:13][C:12]3[C:7]([Cl:6])=[CH:8][C:9]([N:28]4[CH2:29][CH2:30][NH:31][CH2:32][CH2:33]4)=[CH:10][C:11]=3[CH2:17][S:16](=[O:18])(=[O:19])[C:15]=2[CH:20]=1)=[O:27])([CH3:37])[CH3:36]Participants
Conditions
- Temperature
- 90 °C
Procedure
Concentrated sulphuric acid (1 mL) was added dropwise to a stirred solution of compound of Example 18 (0.5 g, 1.18 mmol) in dry isopropanol (50 mL) at 90° C. The reaction mixture was stirred at 90° C. for 2 h. Solvent was removed and the residue was taken in chloroform (100 mL) and this was neutralized using sodium carbonate solution (10%). Chloroform layer was washed with water, brine and dried over sodium sulphate. Solvent was removed and the product obtained was converted to hydrochloride salt by using isopropanol/ethereal-HCl to obtain the title compound. Yield: 0.4 g (67.79%); mp: 262-64° C.; 1H NMR (DMSO-d6, 300 MHz): δ 1.29 (d, 6H, 2CH3), 2.63 (s, 3H, CH3), 3.18 (bs, 4H, 2CH2), 3.44 (bs, 4H, 2CH2), 5.11 (s, 1H, CH), 5.17 (s, 2H, CH2), 7.19 (s, 2H, Ar), 8.07 (s, 1H, Ar), 8.11 (s, 1H, Ar), 9.45 (bs, 2H, NH, HCl); MS: m/e (ES+) 465 (M+1, free base).
Workup
- customSolvent was removed
- washChloroform layer was washed with water, brine
- dry with materialdried over sodium sulphate
- customSolvent was removed
- customthe product obtained
Sources & evidence
- ORD record
- ord-b885b8cb14eb4d3f980b8ae1fcd4eead
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07834052B2
Reaction notes
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