Hydrochloric Acid → HCID 131710489, compound
Reaction equation
[CH3:1][NH:2][C:3]1[C:4]2[C:17]([CH3:18])=[N:16][O:15][C:5]=2[N:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:8]=1.[ClH:19]>C(#N)C>[ClH:19].[CH3:1][NH:2][C:3]1[C:4]2[C:17]([CH3:18])=[N:16][O:15][C:5]=2[N:6]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[CH:8]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
The hydrochloride is prepared by dissolving N, 3-dimethyl-6-phenylisoxazolo[5,4-b]pyridin-4-amine in acetonitrile and adding ethereal hydrochloric acid, yield 88.3%, m.p. 232°-234°.
Sources & evidence
- ORD record
- ord-b85d210d6b334664a2841cbbf9e00f4d
- Source dataset
- uspto-grants-1976_10
- Patent number
- US03985760
Reaction notes
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