Triethylamine → HCID 22228024, compound

HRID 1744553Notes

Reaction equation

HRID 1744553 reaction equation
[CH3:1][N:2]1[CH:6]=[C:5]([C:7](O)=[O:8])[C:4]([CH3:10])=[N:3]1.[NH2:11][C:12]1[CH:13]=[CH:14][C:15]([O:20][CH2:21][C:22]([CH3:25])([CH3:24])[CH3:23])=[C:16]([CH:19]=1)[C:17]#[N:18].C(N(CC)CC)C.P(C#N)(OCC)(OCC)=O>O.CN(C)C=O>[C:17]([C:16]1[CH:19]=[C:12]([NH:11][C:7]([C:5]2[C:4]([CH3:10])=[N:3][N:2]([CH3:1])[CH:6]=2)=[O:8])[CH:13]=[CH:14][C:15]=1[O:20][CH2:21][C:22]([CH3:24])([CH3:23])[CH3:25])#[N:18]

Participants

7

Procedure

1,3-Dimethylpyrazole-4-carboxylic acid (0.6 g), 5-amino-2-neopentyloxybenzonitrile (0.9 g), triethylamine (1.0 g) and diethyl cyanophosphate (1.0 g) were added to dimethylformamide (10 ml) and the mixture was stirred at room temperature for 1 h. The reaction mixture was added into water and extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate, after which the solvent was evaporated under reduced pressure. n-Hexane was added to the residue to allow crystallization. The crystals were recrystallized from hydrous methanol to give the title compound (0.5 g), melting point: 193–194° C.

Workup

  1. extractionextracted with ethyl acetate
  2. washThe organic layer was washed with saturated brine
  3. dry with materialdried over anhydrous magnesium sulfate
  4. customafter which the solvent was evaporated under reduced pressure
  5. additionn-Hexane was added to the residue
  6. customcrystallization
  7. customThe crystals were recrystallized from hydrous methanol

Sources & evidence

ORD record
ord-9cddc13b05f3467cb806ecd00fb47197
Source dataset
uspto-grants-2006_03
Patent number
US07015218B1

Reaction notes

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