Hydrochloric Acid → HCID 67342611, compound
Reaction equation
[CH3:1][C:2]1[N:7]=[N:6][CH:5]=[C:4]([N:8]2[CH2:13][CH2:12][CH:11]([NH:14]C(=O)OC(C)(C)C)[CH2:10][CH2:9]2)[CH:3]=1.[ClH:22]>ClCCl>[ClH:22].[ClH:22].[CH3:1][C:2]1[N:7]=[N:6][CH:5]=[C:4]([N:8]2[CH2:13][CH2:12][CH:11]([NH2:14])[CH2:10][CH2:9]2)[CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution tert-butyl 1-(6-methylpyridazin-4-yl)piperidin-4-ylcarbamate (2.14 g, 7.32 mmol) in dichloromethane (36 mL) was added HCl (2 M in diethylether, 18.3 mL, 36.6 mmol) and the reaction mixture was stirred at room temperature for 24 hours. The mixture was then filtered and the white precipitate was washed with dichloromethane and diethylether and dried to afford the title compound (2.35 g, 82%) as a white solid.
Workup
- filtrationThe mixture was then filtered
- washthe white precipitate was washed with dichloromethane and diethylether
- customdried
Sources & evidence
- ORD record
- ord-dfe9d1ab74a241e4b593f2a339a8eb0e
- Source dataset
- uspto-grants-2013_07
- Patent number
- US08486967B2
Reaction notes
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