Acetonitrile → HCID 86607977, compound

HRID 490773Notes

Reaction equation

HRID 490773 reaction equation
[F:1][C:2]([F:22])([F:21])[C:3]1[CH:4]=[C:5]([N:13]2[C:17]([CH3:18])=[C:16]([CH2:19]Cl)[CH:15]=[N:14]2)[CH:6]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:8]=1.[OH:23][C:24]1[CH:25]=[C:26]2[C:30](=[CH:31][CH:32]=1)[N:29]([C:33]([CH3:38])([CH3:37])[C:34]([OH:36])=[O:35])[CH:28]=[CH:27]2.C([O-])([O-])=O.[Cs+].[Cs+].[C:45](#N)[CH3:46]>>[CH2:45]([O:35][C:34](=[O:36])[C:33]([N:29]1[C:30]2[C:26](=[CH:25][C:24]([O:23][CH2:19][C:16]3[CH:15]=[N:14][N:13]([C:5]4[CH:4]=[C:3]([C:2]([F:22])([F:21])[F:1])[CH:8]=[C:7]([C:9]([F:12])([F:11])[F:10])[CH:6]=4)[C:17]=3[CH3:18])=[CH:32][CH:31]=2)[CH:27]=[CH:28]1)([CH3:38])[CH3:37])[CH3:46]

Participants

5

Procedure

To a solution of 1-(3,5-bis-trifluoromethyl-phenyl)-4-chloromethyl-5-methyl-1H-pyrazole (170 mg, 0.5 mmol) and (2-(5-hydroxy-indol-1-yl)-2-methyl-propionic acid (150 mg) in acetonitrile (3 mL) is added Cs2CO3 (325 mg, 1 mmol). The mixture is stirred at room temperature over night, quenched by water, extracted with ethyl acetate, dried over sodium sulfate. Concentration yields the crude product.

Workup

  1. customquenched by water
  2. extractionextracted with ethyl acetate
  3. dry with materialdried over sodium sulfate
  4. concentrationConcentration

Sources & evidence

ORD record
ord-0c68c61bb9094bc1852362df48d0a7a5
Source dataset
uspto-grants-2009_05
Patent number
US07528160B2

Reaction notes

Loading…