Triethylamine → HCID 18381684, compound

HRID 2297496Notes

Reaction equation

HRID 2297496 reaction equation
[Br-].[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:10](=[CH:11][CH:12]=1)[CH:9]([P+](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)O[C:7]2=[O:32].[N:33]1[CH:38]=[CH:37][C:36]([CH:39]=O)=[CH:35][CH:34]=1.C(N(CC)CC)C.O.[NH2:49][NH2:50]>C(Cl)Cl.O>[CH3:2][O:3][C:4]1[CH:5]=[C:6]2[C:10]([C:9]([CH2:39][C:36]3[CH:37]=[CH:38][N:33]=[CH:34][CH:35]=3)=[N:49][NH:50][C:7]2=[O:32])=[CH:11][CH:12]=1

Participants

7

Procedure

A solution of (5-methoxy-3-oxo-1,3-dihydro-isobenzofuran-1-yl)-triphenyl-phosphonium bromide (43,5 g, 0.0861 mole), prepared as described in example 36, and 4-pyridincarboxaldehyde (9.22 g, 0.0861 mole) in CH2Cl2 (300 ml) was dropwise added with triethylamine (12 ml, 0.0861 mole) while controlling the temperature in water bath. After 1 night under stirring at room temperature, the mixture was washed with water, discoloured, anhydrified and dried. The residue was suspended in CH3OH (135 ml) and added with hydrazine monohydrate (12.55 ml, 0.2583 mole). The mixture was refluxed for 1 hour, then cooled in water/ice, filtered and dried. The residue was crystallised in CH3OH to give 8 g of the title compound. The mother liquors were dried and the residue triturated in CH3OH (50 ml) to give further 3,5 g of the title compound (total yield: 50%).

Workup

  1. washthe mixture was washed with water
  2. customdried
  3. temperatureThe mixture was refluxed for 1 hour
  4. filtrationfiltered
  5. customdried
  6. customThe residue was crystallised in CH3OH

Sources & evidence

ORD record
ord-5bdfa2871a9c41aca259f4d7f3cef723
Source dataset
uspto-grants-2002_12
Patent number
US06492360B1

Reaction notes

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