Dicyclohexylcarbodiimide → HCID 70375209, compound

HRID 1089109Notes

Reaction equation

HRID 1089109 reaction equation
Cl.[CH3:2][N:3]([CH3:8])[CH2:4][C:5](O)=[O:6].N[C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:17]([CH3:23])[CH2:18][C:19](=[O:22])[NH:20][N:21]=2)=[CH:12][CH:11]=1.C1([N:30]=C=NC2CCCCC2)CCCCC1>O.CN(C)C=O>[CH3:2][N:3]([CH2:4][C:5]([C:10]1[CH:15]=[CH:14][C:13]([C:16]2[CH:17]([CH3:23])[CH2:18][C:19](=[O:22])[NH:20][N:21]=2)=[C:12]([NH2:30])[CH:11]=1)=[O:6])[CH3:8]

Participants

6

Procedure

In 1 ml of water was dissolved 0.7 g of N,N-dimethylglycin hydrochloride. This solution was mixed with a solution of 1.0 g of 6-(p-aminophenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone in 20 ml of dimethylformamide. To this mixture was added under ice-cooling 1.2 g of dicyclohexylcarbodiimide, and the reaction was effected for 2 hours. The reaction mixture was allowed to stand for 2 days in a cool place and concentrated under reduced pressure. Water was added to the residue and any insoluble matter was eliminated by filtration. Sodium hydrogen carbonate was added to the filtrate to make it alkaline whereby crystals were precipitated which were then recrystallized from methanol-water to obtain 950 mg of the end product.

Workup

  1. additionTo this mixture was added under ice-
  2. waitto stand for 2 days in a cool place
  3. concentrationconcentrated under reduced pressure
  4. additionWater was added to the residue
  5. filtrationany insoluble matter was eliminated by filtration
  6. additionSodium hydrogen carbonate was added to the filtrate
  7. customwere precipitated which
  8. customwere then recrystallized from methanol-water

Sources & evidence

ORD record
ord-5505538490564767b72222f7cbb4acd0
Source dataset
uspto-grants-1990_10
Patent number
US04965263

Reaction notes

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