Hydrochloric Acid → HCID 21489488, compound
Reaction equation
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]2[C:20]3[N:19]=[C:18]4[CH2:21][CH2:22][CH2:23][N:17]4[CH:16]=[CH:15][C:14]=3[CH:13]=[CH:12][CH2:11]2)=[CH:2]1.[ClH:24]>C(O)C>[ClH:24].[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH:10]2[C:20]3[N:19]=[C:18]4[CH2:21][CH2:22][CH2:23][N:17]4[CH:16]=[CH:15][C:14]=3[CH:13]=[CH:12][CH2:11]2)=[CH:2]1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A portion of the product of Example 3, 12 g., is suspended in 150 ml. of absolute ethanol and treated with one chemical equivalent of 5.02 N ethanolic hydrogen chloride. A clear solution results which is diluted with 200 ml. of anhydrous ether resulting in precipitation of the desired hydrochloride salt. The salt is collected on a filter and recrystallized from a mixture of 150 ml. of ethanol and 150 ml. of ether, yielding 9.3 g. (69.1%) of pure product, m.p. 262°-264° C.
Workup
- customA clear solution results which
- additionis diluted with 200 ml
- customof anhydrous ether resulting in precipitation of the desired hydrochloride salt
- customThe salt is collected on
- filtrationa filter
- customrecrystallized from a mixture of 150 ml
- customof ether, yielding 9.3 g
Sources & evidence
- ORD record
- ord-43890042c1874fe6a5e9ca9ab9c72b30
- Source dataset
- uspto-grants-1976_12
- Patent number
- US04000304
Reaction notes
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