Acetic Anhydride → HCID 69311083, compound

HRID 1243632Notes

Reaction equation

HRID 1243632 reaction equation
[CH:1]1[C:17]2[C:4]([CH:5]=[CH:6][C:7]3[C:16]=2[CH:15]=[C:14]2[C:9](=[CH:10][CH2:11][C:12](=[O:18])[CH2:13]2)[CH:8]=3)=[N:3][N:2]=1.[C:19](OC(=O)C)(=[O:21])[CH3:20]>C(O)(=O)C>[C:19]([N:2]1[CH:1]=[C:17]2[C:4]([CH:5]=[CH:6][C:7]3[CH:8]=[C:9]4[C:14](=[CH:15][C:16]=32)[CH2:13][C:12](=[O:18])[CH:11]=[CH:10]4)=[N:3]1)(=[O:21])[CH3:20]

Participants

4

Reactant 2

HCID 7918Acetic AnhydrideHCID 66612494HCID 66612494, compound

Product 1

HCID 69311083HCID 69311083, compound

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Conditions

Temperature
80 °C

Procedure

Due to limited solubility of Compound 1, purification of the same may be achieved by first derivatizing Compound 1 to a more soluble intermediate, such as the corresponding acetate, recrystallizing the intermediate, and then converting the intermediate to yield purified Compound 1 in good yield. More specifically, to solution of the pyrazoloanthrone (9.67 g, 43.9 mmol) in acetic acid (700 mL) is added acetic anhydride (12.4 mL, 132 mmol). The solution is heated to 80° C. for 5 hours and then cooled to room temperature. After 16 hours, the reaction is cooled to 0° C. for 2 hours. The reaction is then filtered to give the N-acetylpyrazoloanthrone intermediate. This intermediate is recrystallized in acetic acid to give the pure intermediate (5.96 g, 52%). 1H NMR (CDCL3) δ 10.6 (br s, 1H), 8.46 (d, 1H), 8.33 (d, 1H), 8.26 (d, 1H), 8.08 (d, 1H), 7.96–7.87 (m, 2H), 7.78 (t, 1H), 2.83 (s, 3H); ES-MS (m/z) 263 [M+1]+. To a solution of the pure intermediate (5.96 g, 23 mmol) in methanol (600 mL) is added ammonium hydroxide (60 mL). The reaction is stirred at room temperature for 16 hours and then filtered and dried in a vacuum oven. A second crop of crystals is recovered to give a total of 4.8 g of Compound 1 at greater than 98% purity. ES-MS (m/z) 221 [M+1]+.

Workup

  1. customDue to limited solubility of Compound 1, purification of the same
  2. customrecrystallizing the intermediate
  3. customto yield
  4. custompurified Compound 1 in good yield
  5. temperaturecooled to room temperature
  6. temperaturethe reaction is cooled to 0° C. for 2 hours
  7. filtrationThe reaction is then filtered

Sources & evidence

ORD record
ord-6d8195ba9e0b46b2a760e1cbb3d37888
Source dataset
uspto-grants-2006_10
Patent number
US07119114B1

Reaction notes

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