Hydrazine → 2-(4-acetylpiperazinyl)-N-aminoacetamide

HRID 1353835Notes

Reaction equation

HRID 1353835 reaction equation
Br[CH2:2][C:3]([O:5]C)=O.[C:7]([N:10]1[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]1)(=[O:9])[CH3:8].C(=O)([O-])[O-].[K+].[K+].[NH2:22][NH2:23]>C(O)C>[C:7]([N:10]1[CH2:15][CH2:14][N:13]([CH2:2][C:3]([NH:22][NH2:23])=[O:5])[CH2:12][CH2:11]1)(=[O:9])[CH3:8]

Participants

6

Reactant 4

HCID 9321HydrazineHCID 11430Potassium CarbonateHCID 60984Methyl bromoacetate2×HCID 837951-Acetylpiperazine

Product 1

HCID 224797542-(4-acetylpiperazinyl)-N-aminoacetamideYield 80%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
85 °C

Procedure

The procedure described for Example 283 A was followed using methyl bromoacetate (1.5 g, 0.01 mol), 1-acetyl piperazine (1.4 g, 0.011 mol), and potassium carbonate (1.52 g, 0.011 mol). After one day, an additional 0.3 equivalent of methyl bromoacetate was added to the reaction. The crude material was taken up in approximately 2 mL of ethanol and hydrazine was added to the solution (0.25 mL, 0.008 mol). This was heated in a sealed tube at 85° C. for 4 hours. The solvent was removed to yield the title compound (1.6 g, 80% yield). 1H NMR (DMSO-d6) δ 9.0 (s, 1H), 4.2 (br s, 2H), 3.5 (m, 4H), 2.9 (s, 2H), 2.4 (m, 4H), 2.0 (s, 3H).

Workup

  1. customThe solvent was removed

Sources & evidence

ORD record
ord-6af07e2fe9674e4a88e90cfc3b4e3699
Source dataset
uspto-grants-2007_05
Patent number
US07220771B2

Reaction notes

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