2,3-Dichloro-5,6-dicyano-1,4-benzoquinone → HCID 22249950, compound

HRID 890212Notes

Reaction equation

HRID 890212 reaction equation
C(C1C(=O)C(Cl)=C(Cl)C(=O)C=1C#N)#N.[Br:15][C:16]1[C:17]2[CH:43]=[CH:42][CH:41]=[CH:40][C:18]=2[O:19][C:20]=1[C:21]1[C:22]([CH3:39])=[N:23][N:24]2[C:29]3[N:30]([CH:33]([CH2:36][CH3:37])[CH2:34][CH3:35])[CH2:31][CH2:32][C:28]=3[C:27]([CH3:38])=[N:26][C:25]=12>C(Cl)Cl>[Br:15][C:16]1[C:17]2[CH:43]=[CH:42][CH:41]=[CH:40][C:18]=2[O:19][C:20]=1[C:21]1[C:22]([CH3:39])=[N:23][N:24]2[C:29]3[N:30]([CH:33]([CH2:34][CH3:35])[CH2:36][CH3:37])[CH:31]=[CH:32][C:28]=3[C:27]([CH3:38])=[N:26][C:25]=12

Participants

4

Reactant 2

HCID 67752,3-Dichloro-5,6-dicyano-1,4-benzoquinoneHCID 22249795HCID 22249795, compound

Product 1

HCID 22249950HCID 22249950, compoundYield 68.2%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

DDQ (33 mg, 0.15 mmol) was added to a solution of 3-(3-bromobenzo[b]furan-2-yl)-8-(1-ethylpropyl)-2,5-dimethyl-7,8-dihydro-6H-pyrazolo[1,5-a]pyrrolo[3,2-e]pyrimidine (60 mg, 0.13 mmol) in methylene chloride (10 mL) at room temperature, followed by stirring for one hour. After overnight, the residue was purified by silica gel column chromatography (10% ethyl acetate/hexane), to give the title compound (40 mg) as a reddish brown oil.

Workup

  1. waitAfter overnight
  2. customthe residue was purified by silica gel column chromatography (10% ethyl acetate/hexane)

Sources & evidence

ORD record
ord-0294b9c7078e4a1fa7c5f5804ffe0332
Source dataset
uspto-grants-2006_02
Patent number
US06995163B2

Reaction notes

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