Hydrochloric Acid → HCID 86696471, compound
Reaction equation
[ClH:1].[Br:2][C:3]1[N:7]2[N:8]=[C:9]([N:12]3[CH2:17][CH2:16][N:15](C(OC(C)(C)C)=O)[CH2:14][CH:13]3[CH3:25])[CH:10]=[CH:11][C:6]2=[N:5][CH:4]=1>CO>[ClH:1].[ClH:1].[Br:2][C:3]1[N:7]2[N:8]=[C:9]([N:12]3[CH2:17][CH2:16][NH:15][CH2:14][CH:13]3[CH3:25])[CH:10]=[CH:11][C:6]2=[N:5][CH:4]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Concentrated hydrochloric acid (3.0 mL) was added to a solution of tert-butyl 4-(3-bromoimidazo[1,2-b]pyridazin-6-yl)-3-methylpiperazine-1-carboxylate (1.2 g, 3.1 mmol) in methanol (60 mL) and allowed to stir at ambient temperature under N2 blanket for 3d. The solution was then evaporated to dryness to provide 1.1 g of light brown solid. LRMS (ESI) m/z 295.9/297.9 [(M+H)]+, calc'd for C11H14BrN5. 296.17.
Workup
- customThe solution was then evaporated to dryness
- customto provide 1.1 g of light brown solid
Sources & evidence
- ORD record
- ord-2f7348a031dc461988474b7b5b36ba2a
- Source dataset
- uspto-grants-2015_03
- Patent number
- US08969565B2
Reaction notes
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