Isopropyl iodide → HCID 60141761, compound

HRID 2047241Notes

Reaction equation

HRID 2047241 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[C:13]([C:14]([OH:16])=[O:15])=[C:12]([C:17]2[CH:18]=[N:19][N:20]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=3[F:32])[C:21]=2[C:22]([F:25])([F:24])[F:23])[O:11][N:10]=1.[F-].[Cs+].I[CH:36]([CH3:38])[CH3:37]>C(#N)C.ClCCl>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([F:8])[C:3]=1[C:9]1[C:13]([C:14]([O:16][CH:36]([CH3:38])[CH3:37])=[O:15])=[C:12]([C:17]2[CH:18]=[N:19][N:20]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][C:27]=3[F:32])[C:21]=2[C:22]([F:24])([F:25])[F:23])[O:11][N:10]=1

Participants

6

Procedure

3-(2-chloro-6-fluorophenyl)-5-(1-(2-fluorophenyl)-5-(trifluoromethyl)-1H-pyrazol-4-yl)isoxazole-4-carboxylic acid (30 mg, 0.064 mmol), cesium fluoride (12 mg, 0.077 mmol) and 2-iodopropane (0.008 mL, 0.077 mmol) were dissolved in dried acetonitrile (1 mL) and the mixture was refluxed for 20 h. The mixture was diluted with dichloromethane and washed with water. The organic phase was dried over Na2SO4, filtered and the solvent was solvent removed under reduced pressure. The product was purified by pTLC (PE/EE 9/1) to give 26 mg of a yellow oil (yield 79 To). Result of LC/MS [M+H]+: 511.8; 1H NMR (CDCl3): 1.02 (6H, d, 2×CH3), 5.02 (1H, m, CH-propyl), 7.18 (1H, t, CH-arom.), 7.28-7.61 (6H m, CH-arom.), 8.31 (1H, s, CH-pyraz.).

Workup

  1. temperaturethe mixture was refluxed for 20 h
  2. washwashed with water
  3. dry with materialThe organic phase was dried over Na2SO4
  4. filtrationfiltered
  5. customremoved under reduced pressure
  6. customThe product was purified by pTLC (PE/EE 9/1)

Sources & evidence

ORD record
ord-f2eb89f7ad7e428facc392556717cc7c
Source dataset
uspto-grants-2013_11
Patent number
US08592456B2

Reaction notes

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