تفاعل #1340631

ord-0c4c7b52f50b43248a71fe6f8b038445

معادلة التفاعل

CCCC/C(OCC)=C1/C(=O)N(C)N=C1CC(=O)OC
methyl[(4Z)-4-(1-ethoxypentylidene)-1-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate
NCc1ccccn1
1-pyridin-2-ylmethanamine
CCCC/C(NCc1ccccn1)=C1/C(=O)N(C)N=C1CC(=O)OC
methyl[(4Z)-1-methyl-5-oxo-4-{1-[(pyridin-2-ylmethyl)amino]pentylidene}-4,5-dihydro-1H-pyrazol-3-yl]acetate
المردود 92.0%

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    workup.ADDITIONThe mixture of the
  2. 2
    أخرىThe solvent was removed in vacuo
  3. 3
    workup.DISSOLUTIONThe resulting residue was dissolved in a minimum of CH2Cl2
  4. 4
    workup.ADDITIONadded dropwise to a stirred solution of 200 mL of cyclohexane resulting in the formation of a brown precipitate that
  5. 5
    ترشيحwas filtered off

الإجراء التجريبي

The mixture of the above obtained methyl[(4Z)-4-(1-ethoxypentylidene)-1-methyl-5-oxo-4,5-dihydro-1H-pyrazol-3-yl]acetate (Compound of Formula (VII), 1.05 g) and 1-pyridin-2-ylmethanamine (0.262 mL) was stirred at room temperature in toluene (25 mL) for 0.5 h. The solvent was removed in vacuo. The resulting residue was dissolved in a minimum of CH2Cl2 and added dropwise to a stirred solution of 200 mL of cyclohexane resulting in the formation of a brown precipitate that was filtered off. This precipitate was proved to be the pure methyl[(4Z)-1-methyl-5-oxo-4-{1-[(pyridin-2-ylmethyl)amino]pentylidene}-4,5-dihydro-1H-pyrazol-3-yl]acetate (1.20 g). Yield 92%. MS (ESI+): 345.4; MS (ESI−): 342.5.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US08455485B2uspto-grants-2013_06