Ammonia → 2-(dimethoxymethyl)-5-methyl-4-(trifluoromethyl)-1H-imidazole

HRID 43467

Reaction equation

HRID 43467 reaction equation
[CH2:1]1[C:6](=O)[N:5](Cl)C(=O)[CH2:2]1.[F:9][C:10]([F:21])([F:20])C(C1(C)SCCCS1)=O.[CH3:22][O:23][CH:24]([O:27][CH3:28])[CH:25]=O.[NH3:29]>C(#N)C.[N+]([O-])([O-])=O.[Ag+]>[CH3:22][O:23][CH:24]([O:27][CH3:28])[C:25]1[NH:29][C:1]([CH3:2])=[C:6]([C:10]([F:21])([F:20])[F:9])[N:5]=1

Participants

7

Reactant 4

HCID 222AmmoniaHCID 31398ChlorosuccinimideHCID 162650Acetaldehyde, 2,2-dimethoxy-HCID 866484802,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone

Product 1

HCID 675492182-(dimethoxymethyl)-5-methyl-4-(trifluoromethyl)-1H-imidazole

Reagents, catalysts & solvents 2

HCID 24470Silver NitrateCatalystHCID 6342AcetonitrileSolvent

Procedure

NCS (870 mg, 6.51 mmol) and silver nitrate (1.48 g, 8.71 mmol) were dissolved in acetonitrile (40 mL) and distilled water (10 mL). 2,2,2-Trifluoro-1-(2-methyl-1,3-dithian-2-yl)ethanone obtained in Example (36a) (500 mg, 2.17 mmol) was added, and the mixture was stirred for 40 minutes. Thereafter, dimethoxyacetaldehyde (5.76 M aqueous solution, 0.4 mL, 23.0 mmol) and 28% aqueous ammonia (2 mL) were added, and the mixture was stirred at room temperature for 18 hours. The reaction solution was filtered through celite and then concentrated under reduced pressure. The resulting compound was used for the next reaction without purification.

Workup

  1. distillationdistilled water (10 mL)
  2. stirringthe mixture was stirred at room temperature for 18 hours
  3. filtrationThe reaction solution was filtered through celite
  4. concentrationconcentrated under reduced pressure
  5. customThe resulting compound was used for the next reaction without purification

Sources & evidence

ORD record
ord-3540bec67c3547b392f9605095eb2780
Source dataset
uspto-grants-2013_09
Patent number
US08536197B2

Linked notes

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