Dimethyl Sulfoxide → HCID 178437191, compound

HRID 1836301Notes

Reaction equation

HRID 1836301 reaction equation
C(Cl)(=O)C(Cl)=O.CS(C)=O.[NH:11]1[CH2:15][CH:14]([CH:16]([C:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[N:21]=[CH:20][CH:19]=2)[CH3:17])[N:13]=[CH:12]1.C(N(CC)CC)C>ClCCl>[NH:11]1[CH:15]=[C:14]([CH:16]([C:18]2[C:27]3[C:22](=[CH:23][CH:24]=[CH:25][CH:26]=3)[N:21]=[CH:20][CH:19]=2)[CH3:17])[N:13]=[CH:12]1

Participants

6

Procedure

To oxalyl chloride (0.85 μl, 0.976 mmol) in 5 ml of anhydrous dichloromethane at −78° C., dimethylsulfoxide (0.14 ml, 1.95 mmol) was added over a five minute period. After stirring for 5 minutes at the same temperature, 4-[1-(4,5-Dihydro-1H-imidazol-4-yl)-ethyl]quinoline (0.200 g, 0.888 mmol) was added slowly and the reaction mixture was stirred for a further 20 minutes at −78°. Triethylamine (0.62 ml, 4.44 mmol) was added and the reaction mixture was stirred for 5 minutes at −78° C. and then 20 minutes at room temperature. The reaction mixture was concentrated under reduced pressure and partitioned between EtOAc (10 ml) and water (5 ml). The organic layer was dried over sodium sulfate, filtered, concentrated and column purified [EtOAc:MeOH:Methanol NH3 (1.0 M); 3.5:1:0.5) to give 0.100 g (51%) of the product as a syrup.

Workup

  1. additionwas added slowly
  2. stirringthe reaction mixture was stirred for 5 minutes at −78° C.
  3. custom20 minutes
  4. customat room temperature
  5. concentrationThe reaction mixture was concentrated under reduced pressure
  6. custompartitioned between EtOAc (10 ml) and water (5 ml)
  7. dry with materialThe organic layer was dried over sodium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated
  10. customcolumn purified [EtOAc

Sources & evidence

ORD record
ord-87c6db1acbaa41149df09a7efbd6d89c
Source dataset
uspto-grants-2004_08
Patent number
US06777426B2

Reaction notes

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