HCID 54349977, compound → HCID 9826986, compound
Reaction equation
C[O:2][C:3](=[O:36])[CH2:4][CH2:5][C:6]1[S:10][C:9]([CH:11]2[CH2:15][CH2:14][CH2:13][N:12]2[C:16](=[O:35])[CH2:17][C:18]2[CH:23]=[CH:22][C:21]([NH:24][C:25]([NH:27][C:28]3[CH:33]=[CH:32][CH:31]=[CH:30][C:29]=3[CH3:34])=[O:26])=[CH:20][CH:19]=2)=[N:8][CH:7]=1>CO.O1CCCC1.[OH-].[Li+]>[C:29]1([CH3:34])[CH:30]=[CH:31][CH:32]=[CH:33][C:28]=1[NH:27][C:25](=[O:26])[NH:24][C:21]1[CH:20]=[CH:19][C:18]([CH2:17][C:16]([N:12]2[CH2:13][CH2:14][CH2:15][CH:11]2[C:9]2[S:10][C:6]([CH2:5][CH2:4][C:3]([OH:36])=[O:2])=[CH:7][N:8]=2)=[O:35])=[CH:23][CH:22]=1Participants
Reagents, catalysts & solvents 3
Procedure
A solution was prepared of 3-[2-(1-{[4-(3-o-Tolyl-ureido)-phenyl]-acetyl}-pyrrolidin-2-yl)-thiazol-5-yl]-propionic acid methyl ester (0.33 g, 0.65 mmol) in methanol (4 mL), tetrahydrofuran (8 mL) and aqueous lithium hydroxide (2M, 4 mL). The solution was stirred for 4 h and partitioned between aqueous hydrochloric acid (1N, 30 mL) and ethyl acetate (100 mL). The aqueous portion was extracted with ethyl acetate (50 mL). The combined organic portions were extracted with brine (20 mL) and the solvent removed in vacuo to give the title compound (0.3 g, 94%). 1HNMR (400 MHz, CD3OD): δ7.60 (d, J=7.3 Hz, 1H), 7.46 (s, 0.3H), 7.39 (d, J=8.5 Hz, 2.7H), 7.29 (d, J=8.5 Hz, 0.6), 7.18 (m, 3H), 6.99 (m, 1.4H), 5.40 (d, J=7.0 Hz, 0.3H), 5.34 (d, J=6.0 Hz, 0.7H) 3.4-3.8 (m, 4H), 3.05 (m, 2H), 2.60 (m, 2H), 2.27 (s, 3H), 1.9-2.2 (m, 4H). MS: Calc'd for C25H26N4O4S: 492.18. Found: (M+1) 492.9.
Workup
- custompartitioned between aqueous hydrochloric acid (1N, 30 mL) and ethyl acetate (100 mL)
- extractionThe aqueous portion was extracted with ethyl acetate (50 mL)
- extractionThe combined organic portions were extracted with brine (20 mL)
- customthe solvent removed in vacuo
Sources & evidence
- ORD record
- ord-23da08143f884a3182d00e14a404624c
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06306887B1
Reaction notes
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