Hydrochloric Acid → HCID 178458713, compound
Reaction equation
[NH:1]([C:3]1[S:4]/[C:5](=[CH:9]\[C:10]2[CH:11]=[C:12]3[C:17](=[CH:18][CH:19]=2)[N:16]=[CH:15][C:14]([C:20]#[N:21])=[C:13]3[O:22][CH:23]([CH3:25])[CH3:24])/[C:6](=[O:8])[N:7]=1)[NH2:2].[ClH:26]>C(#N)C.O>[ClH:26].[NH:1]([C:3]1[S:4]/[C:5](=[CH:9]\[C:10]2[CH:11]=[C:12]3[C:17](=[CH:18][CH:19]=2)[N:16]=[CH:15][C:14]([C:20]#[N:21])=[C:13]3[O:22][CH:23]([CH3:25])[CH3:24])/[C:6](=[O:8])[N:7]=1)[NH2:2]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
To the solution of 6-[2-hydrazino-4-oxo-4H-thiazol-(5Z)-ylidenemethyl]-4-isopropoxy-quinoline-3-carbonitrile (example 59, 15 mg, 0.042 mmol) in acetonitrile and water (8 mL), hydrochloride acid (1N, 0.17 mL) was added. The reaction completed by stirring the above mixture at room temperature for a short period of time. Then the solvents and excess hydrochloride acid were removed by vacuum and lyophilizer to give 6-[2-hydrazino-4-oxo-4H-thiazol-(5Z)-ylidenemethyl]-4-isopropoxy-quinoline-3-carbonitrile hydrochloride salt. LC-MS m/e 354 (MH+).
Workup
- customThen the solvents and excess hydrochloride acid were removed by vacuum and lyophilizer
Sources & evidence
- ORD record
- ord-c79223a2fabb44d9b7d2ea8700e7a8c3
- Source dataset
- uspto-grants-2007_07
- Patent number
- US07250515B2
Reaction notes
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