8-Chloro-3-ethyl-[1,2,4]triazolo[4,3-A]pyrazine → 3-Ethyl-5,6,7,8-tetrahydro-[1,2,4]triazolo[4,3-a]pyrazine hydrochloride
Reaction equation
[Cl:1][C:2]1[C:3]2[N:4]([C:8]([CH2:11][CH3:12])=[N:9][N:10]=2)[CH:5]=[CH:6][N:7]=1>CO.[Pt]=O>[ClH:1].[CH2:11]([C:8]1[N:4]2[CH2:5][CH2:6][NH:7][CH2:2][C:3]2=[N:10][N:9]=1)[CH3:12]Participants
4
Procedure
The title compound was prepared from 8-chloro-3-ethyl-1,2,4-triazolo[4,3-α]pyrazine (2.70 g, 14.8 mmol, from Step A) and platinum oxide (0.4 g) in 200 mL of methanol in a paar shaker under hydrogen (50 psi) for 14 hours. Filtration through Celite followed by concentration gave the title compound as a solid.
Workup
- filtrationFiltration through Celite
- concentrationfollowed by concentration
Sources & evidence
- ORD record
- ord-240b33ea44a44b4a9e30c0f4f1605bdb
- Source dataset
- uspto-grants-2006_10
- Patent number
- US07125873B2
Reaction notes
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