Hydrazine → 6-(Aminomethyl)-1,2,4-triazin-5(4H)-one
Reaction equation
[O:1]=[C:2]1[C:7]([CH2:8][N:9]2C(=O)C3C(=CC=CC=3)C2=O)=[N:6][N:5]=[CH:4][NH:3]1.NN>C(Cl)Cl.CCO>[NH2:9][CH2:8][C:7]1[C:2](=[O:1])[NH:3][CH:4]=[N:5][N:6]=1Participants
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A slurry of 2-(5-oxo-4,5-dihydro-[1,2,4]triazin-6-ylmethyl)-isoindole-1,3-dione (4 g, 15.6 mmol) in CH2Cl2/EtOH (1:1) (150 mL ) was charged with anhydrous hydrazine (1.23 mL, 39.0 mmol) and stirred at rt for 18 h. The reaction mixture was concentrated in vacuo and the off-white solid was triturated with warm CHCl3 and filtered through a fritted funnel. The solid was then triturated with hot methanol (MeOH) and filtered through a fritted funnel resulting in an off-white solid. The material was triturated a second time as before and dried overnight resulting in the title compound as a white solid, which was taken on to the next step without further purification; 1H NMR (DMSO-d6, 400 MHz) δ 3.88(s, 2H), 8.31 (2, 1H); MS (ES+): m/z 127.07 (100) [MH+], HPLC: tR=0.34 min (MicromassZQ, polar—5 min).
Workup
- concentrationThe reaction mixture was concentrated in vacuo
- customthe off-white solid was triturated with warm CHCl3
- filtrationfiltered through a fritted funnel
- customThe solid was then triturated with hot methanol (MeOH)
- filtrationfiltered through a fritted funnel
- customresulting in an off-white solid
- customThe material was triturated a second time as before and
- customdried overnight
Sources & evidence
- ORD record
- ord-773fc048e4b244d4b9c0484ef8eb6ed7
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741324B2
Reaction notes
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