Water → HCID 66885880, compound

HRID 916679Notes

Reaction equation

HRID 916679 reaction equation
Br[CH2:2][C:3]1[N:7]([C:8]2[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][CH:9]=2)[C:6]([C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=2[Cl:22])=[N:5][C:4]=1[C:23]([O:25][CH2:26][CH3:27])=[O:24].[CH:28]([N:31]([CH:34]([CH3:36])C)CC)([CH3:30])C.N1CCCC1.O>C(#N)C>[Cl:14][C:11]1[CH:12]=[CH:13][C:8]([N:7]2[C:3]([CH2:2][N:31]3[CH2:28][CH2:30][CH2:36][CH2:34]3)=[C:4]([C:23]([O:25][CH2:26][CH3:27])=[O:24])[N:5]=[C:6]2[C:15]2[CH:20]=[CH:19][C:18]([Cl:21])=[CH:17][C:16]=2[Cl:22])=[CH:9][CH:10]=1

Participants

6

Procedure

Part B: To a magnetically stirred solution of ethyl 5-bromomethyl-1-(4-chlorophenyl)-2-(2,4-dichlorophenyl)-1H-imidazole4-carboxylate (11.69 g, 23.9 mmol) in acetonitrile (40 ml) is added diisopropylethylamine (DIPEA) (5.2 ml, 30 mmol) and pyrrolidine (1.7 g, 23.9 mmol) and the resulting solution is reacted at room temperature for 2 hours. Water (250 ml) is added and the resulting mixture is extracted three times with dichloromethane. The collected dichloromethane layers are dried over Na2SO4, filtered and concentrated in vacuo. Subsequent purification with flash chromatography (petroleum ether/EtOAC=20/80 (v/v)) gives ethyl 1-(4-chlorophenyl)-2-(2,4-dichloro-phenyl)-5(pyrrolidin-1-ylmethyl)-1H-imidazole-4-carboxylate (3.7 gram, 32% yield). 1H-NMR (200 MHz, CDCl3): δ 1.42 (t, J=7 Hz, 3H), 1.62-1.72 (m, 4H), 2.42-2.50 (m, 4H), 3.83 (s, 2H), 4.43 (q, J=7 Hz, 2H), 7.17-7.40 (m, 7H).

Workup

  1. customthe resulting solution is reacted at room temperature for 2 hours
  2. extractionthe resulting mixture is extracted three times with dichloromethane
  3. dry with materialThe collected dichloromethane layers are dried over Na2SO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customSubsequent purification with flash chromatography (petroleum ether/EtOAC=20/80 (v/v))

Sources & evidence

ORD record
ord-a0228f59ea5149db8e258e0e5b511178
Source dataset
uspto-grants-2007_09
Patent number
US07271189B2

Reaction notes

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