Hydrochloric Acid → Ammonia
Reaction equation
[CH:1]1([NH:4][C:5]([C:7]2[CH:8]=[CH:9][C:10]([CH3:35])=[C:11]([C:13]3[CH:34]=[CH:33][C:16]4[C:17]([N:20]5[CH2:25][CH2:24][N:23](C(OC(C)(C)C)=O)[CH2:22][CH2:21]5)=[N:18][O:19][C:15]=4[CH:14]=3)[CH:12]=2)=[O:6])[CH2:3][CH2:2]1.Cl>CO.O1CCOCC1>[NH3:4].[CH:1]1([NH:4][C:5](=[O:6])[C:7]2[CH:8]=[CH:9][C:10]([CH3:35])=[C:11]([C:13]3[CH:34]=[CH:33][C:16]4[C:17]([N:20]5[CH2:25][CH2:24][NH:23][CH2:22][CH2:21]5)=[N:18][O:19][C:15]=4[CH:14]=3)[CH:12]=2)[CH2:2][CH2:3]1Participants
6
Reactant 2
Product 2
Reagents, catalysts & solvents 2
Procedure
A solution of 1,1-dimethylethyl 4-(6-{5-[(cyclopropylamino)carbonyl]-2methylphenyl}-1,2-benzisoxazol-3-yl)-1-piperazinecarboxylate (Intermediate 26) in methanol (1 ml) was treated with a solution of hydrogen chloride in dioxan (4N, 1 ml) then stirred at room temp. for 18 h. The solvent was evaporated and the residue was re-dissolved in methanol and applied to an SCX cartridge (1 g). Elution with methanol followed by methanol:0.88 ammonia (99:1) gave the title compound as a white solid (0.016 g).
Workup
- customThe solvent was evaporated
- dissolutionthe residue was re-dissolved in methanol
- washElution with methanol
Sources & evidence
- ORD record
- ord-2ce5580b1c7a4e349ae14181ef5dc6f1
- Source dataset
- uspto-grants-2010_01
- Patent number
- US07642276B2
Reaction notes
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