Bromocyclopentane → HCID 68295537, compound

HRID 1909333Notes

Reaction equation

HRID 1909333 reaction equation
[C:1]([N:4]1[C:12]2[CH:11]=[C:10]([C:13]([F:16])([F:15])[F:14])[CH:9]=[C:8]([C:17]([O:19][CH3:20])=[O:18])[C:7]=2[CH:6]=[N:5]1)(=O)[CH3:2].C(=O)([O-])[O-].[Cs+].[Cs+].Br[CH:28]1[CH2:32]CC[CH2:29]1>C(#N)C>[CH:1]1([N:4]2[C:12]3[CH:11]=[C:10]([C:13]([F:16])([F:15])[F:14])[CH:9]=[C:8]([C:17]([O:19][CH3:20])=[O:18])[C:7]=3[CH:6]=[N:5]2)[CH2:32][CH2:28][CH2:29][CH2:2]1

Participants

5

Reactant 3

HCID 8728BromocyclopentaneHCID 10796Cesium carbonateHCID 68295765HCID 68295765, compound

Product 1

HCID 68295537HCID 68295537, compoundYield 30%

Reagents, catalysts & solvents 1

HCID 6342AcetonitrileSolvent2×

Conditions

Temperature
90 °C

Procedure

To a stirred solution of methyl 1-acetyl-6-(trifluoromethyl)-1H-indazole-4-carboxylate (1 equiv.) in acetonitrile (3 mL per 1 mmol), cesium carbonate (1.5 equiv.) was added followed by bromocyclopentane (2 equiv.). The reaction mixture was stirred at 90° C. for 3-4 h. On completion of reaction, acetonitrile was removed under reduced pressure and water was added. Extraction was carried out using ethyl acetate and the combined organic layers washed with water, brine and dried over anhydrous Na2SO4. Solvent was removed under reduced pressure and residue was purified by silica gel column chromatography to obtain methyl 1-cyclopentyl-6-(trifluoromethyl)-1H-indazole-4-carboxylate (yield 30-35%). The structure was confirmed as the desired regioisomer by NOE.

Workup

  1. customwas removed under reduced pressure and water
  2. additionwas added
  3. extractionExtraction
  4. washthe combined organic layers washed with water, brine
  5. dry with materialdried over anhydrous Na2SO4
  6. customSolvent was removed under reduced pressure and residue
  7. customwas purified by silica gel column chromatography

Sources & evidence

ORD record
ord-d12b71b4e262462799ac66858935a18e
Source dataset
uspto-grants-2013_12
Patent number
US08598167B1

Reaction notes

Loading…