Hydrochloric Acid → 3-(1H-Pyrazol-1-yl)-5,6,7,8-tetrahydro[1,2,4]triazolo[4,3-a]pyrazine
Reaction equation
[N:1]1([C:6]2[N:10]3[CH2:11][CH2:12][N:13](C(OC(C)(C)C)=O)[CH2:14][C:9]3=[N:8][N:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1.Cl>>[N:1]1([C:6]2[N:10]3[CH2:11][CH2:12][NH:13][CH2:14][C:9]3=[N:8][N:7]=2)[CH:5]=[CH:4][CH:3]=[N:2]1Participants
3
Procedure
A mixture of 1,1-dimethylethyl 3-(1H-pyrazol-1-yl)-5,6-dihydro[1,2,4]triazolo[4,3-a]pyrazine-7(8H)-carboxylate (I106) (24 mg, 0.083 mmol) and HCl (2 ml, 8.00 mmol) was stirred at room temp for 40 mins. The solvent was evaporated and the product was passed through SCX (elution with 2 M NH3 in methanol) to give the desired product as a white solid.
Workup
- customThe solvent was evaporated
- washthe product was passed through SCX (elution with 2 M NH3 in methanol)
Sources & evidence
- ORD record
- ord-85ce28f9bc0b4632833f3a346ca26bb3
- Source dataset
- uspto-grants-2013_08
- Patent number
- US08501946B2
Reaction notes
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