Dimethylamine → 4-Chloro-3-(3-{[5-cyano-2-propyl-4-(trifluoromethyl)-1h-indol-1-yl]methyl}-1,2,4-oxadiazol-5-yl)-n,n-dimethylbenzamide

HRID 2102117Notes

Reaction equation

HRID 2102117 reaction equation
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][C:3]=1[C:11]1[O:15][N:14]=[C:13]([CH2:16][N:17]2[C:25]3[C:20](=[C:21]([C:28]([F:31])([F:30])[F:29])[C:22]([C:26]#[N:27])=[CH:23][CH:24]=3)[CH:19]=[C:18]2[CH2:32][CH2:33][CH3:34])[N:12]=1.[NH:35]([CH3:37])[CH3:36]>C1COCC1>[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([N:35]([CH3:37])[CH3:36])=[O:7])=[CH:4][C:3]=1[C:11]1[O:15][N:14]=[C:13]([CH2:16][N:17]2[C:25]3[C:20](=[C:21]([C:28]([F:29])([F:30])[F:31])[C:22]([C:26]#[N:27])=[CH:23][CH:24]=3)[CH:19]=[C:18]2[CH2:32][CH2:33][CH3:34])[N:12]=1

Participants

4

Reactant 2

HCID 674DimethylamineHCID 578000844-Chloro-3-(3-{[5-cyano-2-propyl-4-(trifluoromethyl)-1H-indol-1-yl]methyl}-1,2,4-oxadiazol-5-yl)benzoyl chloride

Product 1

HCID 578003664-Chloro-3-(3-{[5-cyano-2-propyl-4-(trifluoromethyl)-1h-indol-1-yl]methyl}-1,2,4-oxadiazol-5-yl)-n,n-dimethylbenzamideYield 66%

Reagents, catalysts & solvents 1

HCID 8028TetrahydrofuranSolvent

Procedure

A round bottom flask was mixed with 4-chloro-3-(3-{[5-cyano-2-propyl-4-(trifluoromethyl)-1H-indol-1-yl]methyl}-1,2,4-oxadiazol-5-yl)benzoyl chloride (Example 295B) (0.037 g, 0.07 mmol) and Me2NH (2.0 mL), and THF (5.0 mL). The mixture was stirred at rt for 2 h and concentrated to dryness. The resulting solid was crystallized with Et2O, filtered in vacuo and dried under high vacuum to afford a pure solid (0.025 g, 66% yield): MS (ES) m/z 515 (M+).

Workup

  1. concentrationconcentrated to dryness
  2. customThe resulting solid was crystallized with Et2O
  3. filtrationfiltered in vacuo
  4. customdried under high vacuum

Sources & evidence

ORD record
ord-6f77a5e5ed404dea82ca0bce61c52297
Source dataset
uspto-grants-2009_08
Patent number
US07572820B2

Reaction notes

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