Sodium Acetate → HCID 18176138, compound

HRID 507489Notes

Reaction equation

HRID 507489 reaction equation
[C:1]([O-])(=[O:3])[CH3:2].[Na+].[Br:6][C:7]1[CH:8]=[C:9]([NH:13][C:14]2[C:23]3[C:18](=[CH:19][CH:20]=[C:21]([NH:24][C:25]([CH:27]=[CH:28][C:29](O)=[O:30])=[O:26])[CH:22]=3)[N:17]=[CH:16][N:15]=2)[CH:10]=[CH:11][CH:12]=1>C(OC(=O)C)(=O)C>[Br:6][C:7]1[CH:8]=[C:9]([N:13]([C:14]2[C:23]3[C:18](=[CH:19][CH:20]=[C:21]([N:24]4[C:29](=[O:30])[CH:28]=[CH:27][C:25]4=[O:26])[CH:22]=3)[N:17]=[CH:16][N:15]=2)[C:1](=[O:3])[CH3:2])[CH:10]=[CH:11][CH:12]=1

Participants

4

Reactant 2

HCID 517045Sodium AcetateHCID 53786874HCID 53786874, compound

Product 1

HCID 18176138HCID 18176138, compoundYield 39%

Reagents, catalysts & solvents 1

HCID 7918Acetic AnhydrideSolvent

Procedure

Sodium acetate (0.10 g, 1.2 mmol) was added to a suspension of 3-[4-(3-bromo-phenylamino)-quinazolin-6-ylcarbamoyl]-acrylic acid (Z) (0.25 g, 0.61 mmol) in 5 mL of acetic anhydride, and the mixture was heated under reflux for 30 minutes. After cooling to room temperature, the reaction was filterd and the filtrate concentrated to dryness in vacuo. The residue was taken up in EtOAc and washed sequentially with saturated sodium bicarbonate, water, and brine. The EtOAc portion was dried over magnesium sulfate, filtered and concentrated to afford a faintly pink solid. The solid was recrystallized twice from EtOAc to afford N-(3-bromo-phenyl)-N-[6-(2,5-dioxo-2,5-dihydro-pyrrol-1-yl)-quinazolin-4-yl]-acetamide (0.104 g, 39%) as an off-white powder, mp 174-175° C.

Workup

  1. temperaturethe mixture was heated
  2. temperatureunder reflux for 30 minutes
  3. concentrationthe filtrate concentrated to dryness in vacuo
  4. washwashed sequentially with saturated sodium bicarbonate, water, and brine
  5. dry with materialThe EtOAc portion was dried over magnesium sulfate
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customto afford a faintly pink solid
  9. customThe solid was recrystallized twice from EtOAc

Sources & evidence

ORD record
ord-2e15b6e068f940aa8a51b692c55fdfa9
Source dataset
uspto-grants-2010_08
Patent number
US07786131B2

Reaction notes

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