Water → HCID 86756495, compound

HRID 1071710Notes

Reaction equation

HRID 1071710 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]1

Participants

6

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

  1. extractionthe mixture extracted with ethyl acetate (3×100 mL)
  2. washThe combined organic extracts were washed with 50 mL of brine
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo

Sources & evidence

ORD record
ord-f0df8f3e9d064e339f86a1987de896aa
Source dataset
uspto-grants-2005_06
Patent number
US06906082B2

Reaction notes

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