Acetic Acid → HCID 10076548, compound
Reaction equation
[CH2:1]([N:5]([C:34](=[O:41])[CH2:35][C:36]([O:38]CC)=[O:37])[C:6]1[CH:11]=[CH:10][C:9]([N:12]2[CH2:17][CH2:16][CH:15]([NH:18][CH2:19][C@H:20]([OH:33])[C:21]3[CH:26]=[CH:25][C:24]([OH:27])=[C:23]([NH:28][S:29]([CH3:32])(=[O:31])=[O:30])[CH:22]=3)[CH2:14][CH2:13]2)=[CH:8][CH:7]=1)[CH2:2][CH2:3][CH3:4].[OH-].[Na+].C(O)(=O)C>O.C(O)C>[CH2:1]([N:5]([C:34](=[O:41])[CH2:35][C:36]([OH:38])=[O:37])[C:6]1[CH:7]=[CH:8][C:9]([N:12]2[CH2:17][CH2:16][CH:15]([NH:18][CH2:19][C@H:20]([OH:33])[C:21]3[CH:26]=[CH:25][C:24]([OH:27])=[C:23]([NH:28][S:29]([CH3:32])(=[O:31])=[O:30])[CH:22]=3)[CH2:14][CH2:13]2)=[CH:10][CH:11]=1)[CH2:2][CH2:3][CH3:4]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 2
Procedure
To a stirred solution of ethyl 3-(butyl-4-{4-[((2R)-2-hydroxy-2-{4-hydroxy-3-l}ethyl)amino]-1-piperidineyl}anilino)-3-oxopropanoate (which was obtained in Example 373) (0.23 g, 0.39 mmol) in distilled water (3 mL) and ethanol (2 mL) was added 1 N sodium hydroxide (2 mL). The reaction was stirred at room temperature for 1 hour. The mixture was acidified (pH 6) with glacial acetic acid, concentrated, triturated with water, ethyl acetate, ether, and dried under vacuum to give the titled compound as a tan solid (0.04 g, 19%); 1H NMR (300 MHz, DMSO-d6) δ 1.20-1.50 (m, 6H), 1.70-1.95 (m, 2H), 2.60-2.80 (m, 5H), 2.83 (s, 2H), 2.91 (s, 3H), 3.45-3.70 (m, 4H), 4.55-4.65 (m, 1H), 6.81 (d, J=8.0 Hz, 1H), 6.90 (d, J=8.7 Hz, 2H), 7.09 (d, J=8.7 Hz, 2H), 7.07 (s, 1H); MS (ES) m/z: 563.2 (MH+); HRMS Calcd. for C27H39N4O7S(MH+): 563.2461. Found: 563.2526.
Workup
- concentrationconcentrated
- customtriturated with water, ethyl acetate, ether
- customdried under vacuum
Sources & evidence
- ORD record
- ord-c119407786354efeb7d04d66f472f697
- Source dataset
- uspto-grants-2003_02
- Patent number
- US06525202B2
Reaction notes
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