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Chemical Structure| 851726-65-3 Chemical Structure| 851726-65-3

Structure of 851726-65-3

Chemical Structure| 851726-65-3

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Product Details of [ 851726-65-3 ]

CAS No. :851726-65-3
Formula : C13H14N2O3
M.W : 246.26
SMILES Code : O=C(N1CC(N(C)C=C1)=O)OCC2=CC=CC=C2

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Application In Synthesis of [ 851726-65-3 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 851726-65-3 ]

[ 851726-65-3 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 851726-65-3 ]
  • [ 59702-07-7 ]
YieldReaction ConditionsOperation in experiment
Step 3: l-methylpiperazin-2-one; A mixture of 4-benzyloxycarbonyl-l-methyl-3,4-dihydropyrazin-2(lH)-one (510 g, 2.1 mol) and 10% Pt/C (40 g) in ethanol (12 L) was stirred under an atmosphere of hydrogen (1 atm) at room temperature overnight. Pearlmans catalyst (50 g; 20% Pd(OH)2 on C) was added and stirred under an atmosphere of hydrogen gas for additional 24 hours. The product mixture was filtered through a pad of Celite, and concentrated under vacuum to provide l-methylpiperazin-2-one. lH NMR (400 MHz, CDCI3) delta 3.52 (s, 2H), 3.32 (t, J= 5.7 Hz, 2H) 3.09 (t, J= 5.7 Hz, 2H), 2.97 (s, 3H).
A mixture of 4-benzyloxycarbonyl-l-methyl-3, 4-dihydropyrazin-2 (1H)-one (510 g, 2. 1mol) and 10% Pt/C (40 g) in ethanol (12 L) was stirred under an atmosphere of hydrogen (1 atm) at room temperature overnight. Pearlmans catalyst (50 g; 20% Pd (OH) 2 on C) was added and stirred under an atmosphere of hydrogen gas for additional 24 hours. The product mixture was filtered through a pad of Celite, and concentrated under vacuum to provide l-methylpiperazin-2-one. 1H NMR (400 MHz, CDC13) 8 3.52 (s, 2H), 3.32 (t, J = 5.7 Hz, 2H) 3.09 (t, J = 5.7 Hz, 2H), 2.97 (s, 3H).
A mixture of 4-benzyloxycarbonyl-1-methyl-3,4-dihydropyrazin-2(1Fn-one (510 g, 2.1mol) and 10% Pt/C (40 g) in ethanol (12 L) was stirred under an atmosphere of hydrogen (1 atm) at room temperature overnight. Pearlman's catalyst (50 g; 20% Pd (OH)2 C) was added and stirred under an atmosphere of hydrogen gas for additional 24 hours. The product mixture was filtered through a pad of Celite, and then concentrated under vacuum to provide 1-methylpiperazin-2-one. ¹H NMR (400 MHz, CDCI3) 8 3.52 (s, 2H), 3.32 (t, J = 5.7 Hz, 2H) 3.09 (t, J = 5.7 Hz, 2H), 2.97 (s, 3H).
 

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