Water → HCID 86756495, compound
Reaction equation
[CH3:1][O:2][C:3](=[O:43])[N:4]([CH2:28][C:29]1[CH:34]=[C:33]([C:35]([F:38])([F:37])[F:36])[CH:32]=[C:31]([C:39]([F:42])([F:41])[F:40])[CH:30]=1)[C@H:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:15]([F:18])([F:17])[F:16])[CH:13]=2)[N:8](C(=O)C(F)(F)F)[C@@H:7]([CH:25]2[CH2:27][CH2:26]2)[CH2:6]1.O1CCCC1.[OH-].[Li+].O>CO>[F:38][C:35]([F:36])([F:37])[C:33]1[CH:34]=[C:29]([CH:30]=[C:31]([C:39]([F:41])([F:42])[F:40])[CH:32]=1)[CH2:28][N:4]([C:3]([O:2][CH3:1])=[O:43])[C@H:5]1[C:14]2[C:9](=[CH:10][CH:11]=[C:12]([C:15]([F:18])([F:17])[F:16])[CH:13]=2)[NH:8][C@@H:7]([CH:25]2[CH2:27][CH2:26]2)[CH2:6]1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Procedure
cis-(3,5-Bis-trifluoromethyl-benzyl)-(2-cyclopropyl-1-trifluoroacetyl-6-trifluoromethyl-1,2,3,4-tetrahydro-quinolin-4-yl)-carbamic acid methyl ester (Example 47) (900 mg, 1.41 mmol) was dissolved in 20 mL of methanol and 60 mL of tetrahydrofuran before adding lithium hydroxide (1.6 mL of 1.0M aqueous solution, 1.6 mmol) to the solution. After 2 h at room temperature, 100 mL of water was added and the mixture extracted with ethyl acetate (3×100 mL). The combined organic extracts were washed with 50 mL of brine, dried over sodium sulfate, filtered and concentrated in vacuo to afford the title product (740 mg) as a colorless solid which was used without further purification. MS m/z 542 (M+2)+; 1H NMR (CDCl3) δ 0.2 (m, 2H), 0.55 (m, 2H), 0.8 (m, 1H).
Workup
- extractionthe mixture extracted with ethyl acetate (3×100 mL)
- washThe combined organic extracts were washed with 50 mL of brine
- dry with materialdried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated in vacuo
Sources & evidence
- ORD record
- ord-f0df8f3e9d064e339f86a1987de896aa
- Source dataset
- uspto-grants-2005_06
- Patent number
- US06906082B2
Reaction notes
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