Water → HCID 15580723, compound

HRID 1702650Notes

Reaction equation

HRID 1702650 reaction equation
F[C:2](F)(F)[C:3]([NH:5][C:6]1[CH:10]([CH3:11])[CH2:9][N:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:7]=1)=[O:4].C(OC(=O)C)(=O)C.O>CN(C)C1C=CN=CC=1.ClCCl>[CH3:11][CH:10]1[CH2:9][N:8]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)[N:7]=[C:6]1[NH:5][C:3](=[O:4])[CH3:2]

Participants

6

Procedure

A 10.0 g. amount of 3-amino-4-methyl-1-phenyl-2-pyrazoline (prepared as described in Example 6) is dissolved in 50 ml. of acetic anhydride, then 500 mg. of 4-dimethylaminopyridine is added and the reaction mixture is allowed to stand at room temperature for 18 hours. The mixture is poured into water to separate a gum which solidifies and is collected by filtration. The solid is added with stirring to 150 ml. of methanol containing 10.0 g. of sodium hydroxide. After 30 minutes, the solvent is removed in vacuo and water is added to provide a gum which becomes solid. This solid is dissolved in dichloromethane, dried over anhydrous magnesium sulfate and passed through a short column of a hydrous magnesium silicate. The effluent is concentrated while adding hexane to yield crystals. The material is collected and dried to give 3.3 g. of the desired product as a white solid, m.p. 149°-150° C.

Workup

  1. customto separate a gum which
  2. filtrationis collected by filtration
  3. additionThe solid is added
  4. waitAfter 30 minutes
  5. customthe solvent is removed in vacuo and water
  6. additionis added
  7. customto provide a gum which
  8. dry with materialdried over anhydrous magnesium sulfate
  9. concentrationThe effluent is concentrated
  10. additionwhile adding hexane
  11. customto yield crystals
  12. customThe material is collected
  13. customdried
  14. customto give 3.3 g

Sources & evidence

ORD record
ord-ca9f5e7ba11248ad818d905af6e22d4c
Source dataset
uspto-grants-1982_09
Patent number
US04348527

Reaction notes

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