Ethyl Acetate → HCID 69041919, compound

HRID 433574Notes

Reaction equation

HRID 433574 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[CH:13]=[C:12]([CH2:14][N:15]3[CH:19]=[CH:18][N:17]=[C:16]3[NH2:20])[N:11]=[CH:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8].[BH4-].[Na+].[CH3:23]COC(C)=O>C(OCC)(OCC)OCC.[Cl-].[Na+].O>[ClH:1].[Cl:1][C:2]1[CH:3]=[C:4]([N:9]2[CH:13]=[C:12]([CH2:14][N:15]3[CH:19]=[CH:18][N:17]=[C:16]3[NH:20][CH3:23])[N:11]=[CH:10]2)[CH:5]=[CH:6][C:7]=1[Cl:8]

Participants

6

Reactant 3

HCID 8857Ethyl AcetateHCID 4311764Sodium borohydrideHCID 69040616HCID 69040616, compound

Product 1

HCID 69041919HCID 69041919, compound

Reagents, catalysts & solvents 2

HCID 31214Ethyl orthoformateSolventHCID 57417360Sodium chloride; waterSolvent

Procedure

A suspension of 1-[1-(3,4-dichloro-phenyl)-1H-imidazol-4-ylmethyl]-1H-imidazol-2-ylamine (0.7 g, 2.3 mmol) in triethyl orthoformate (10 ml) was stirred under reflux for 2 h. The reaction mixture was evaporated to dryness, dissolved in ethanol (10 ml) and cooled in an ice bath. Sodium borohydride (0.091 g, 2.4 mmol) was added and the mixture was allowed to slowly reach 20° C. After 18 h AcOEt and brine was added and the organic phase was separated, dried (Na2SO4) and concentrated. After chromatography [silica, elution with gradient CH2Cl2 to 100% (CH2Cl2/MeOH/aq. NH4OH=90:10:1)] the free base of the title compound was obtained. It was crystallized as the off-white hydrochloride salt (0.25 g; 16%). Mp. >250° C. (MeOH/Et2O), MS: m/e=322 (M+H+).

Workup

  1. temperatureunder reflux for 2 h
  2. customThe reaction mixture was evaporated to dryness
  3. dissolutiondissolved in ethanol (10 ml)
  4. temperaturecooled in an ice bath
  5. customwas allowed to slowly reach 20° C
  6. customthe organic phase was separated
  7. dry with materialdried (Na2SO4)
  8. concentrationconcentrated
  9. washAfter chromatography [silica, elution with gradient CH2Cl2 to 100% (CH2Cl2/MeOH/aq. NH4OH=90:10:1)] the free base of the title compound
  10. customwas obtained
  11. customIt was crystallized as the off-white hydrochloride salt (0.25 g; 16%)

Sources & evidence

ORD record
ord-af40f3f0dda44c8bb69ffe21e1dbf6ad
Source dataset
uspto-grants-2003_12
Patent number
US06667335B2

Reaction notes

Loading…