Water → HCID 178514960, compound

HRID 612984Notes

Reaction equation

HRID 612984 reaction equation
[NH2:1][C:2]1[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([Cl:14])=[CH:9][C:8]=2[Cl:15])[N:5]=[C:4]([OH:16])[CH:3]=1.[C:17]1(=O)[O:22][C:20](=[O:21])[C:19]2=[CH:23][CH:24]=[CH:25][CH:26]=[C:18]12.O>C(O)(=O)C>[OH:16][C:4]1[CH:3]=[C:2]([N:1]2[C:20](=[O:21])[C:19]3=[CH:23][CH:24]=[CH:25][CH:26]=[C:18]3[C:17]2=[O:22])[N:6]([C:7]2[C:12]([Cl:13])=[CH:11][C:10]([Cl:14])=[CH:9][C:8]=2[Cl:15])[N:5]=1

Participants

5

Procedure

A mixture of 4.50 g (18.0 mmol) of the compound of Step A and 2.81 g (19.0 mmol) of phthalic anhydride in 40 mL of glacial acetic acid was refluxed for 4 hours and stirred overnight at room temperature. About two volumes of water were added dropwise and the resulting solid was filtered and washed with water. The damp solid was taken up in a little ethanol, filtered and washed with a little ethanol and ether, and air dried to give the title compound, 5.11 g (69%), m.p. 295-298° C.(dec). Anal. Calcd. for C17H8O3N3Cl3 : C, 49.97; H, 1.97; N. 10.28. Found: C, 49.28; H, 1.95; N, 10.06.

Workup

  1. temperaturewas refluxed for 4 hours
  2. filtrationthe resulting solid was filtered
  3. washwashed with water
  4. filtrationfiltered
  5. washwashed with a little ethanol and ether, and air
  6. customdried

Sources & evidence

ORD record
ord-f72c4d090b944f13b7581b0969ab9fd7
Source dataset
uspto-grants-1999_12
Patent number
US06005109

Reaction notes

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