Hydrochloric Acid → HCID 22350951, compound
Reaction equation
[CH3:1][C:2]1[S:6][C:5](=[N:7][C:8]2[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=2)[N:4]([CH2:14][CH2:15][CH2:16][NH:17]C(=O)OC(C)(C)C)[C:3]=1[C:25]1[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=1.Cl>O1CCOCC1>[NH2:17][CH2:16][CH2:15][CH2:14][N:4]1[C:3]([C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[C:2]([CH3:1])[S:6][C:5]1=[N:7][C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
t-Butyl 3-[5-methyl-4-phenyl-2-(phenylimino)thiazol-3(2H)-yl]propylcarbamate (370 mg) and a 4N solution of hydrogen chloride in dioxane (4 ml) were treated in a similar manner to in Example 9. (2) to give the title compound (327 mg) as hydrochloride.
Sources & evidence
- ORD record
- ord-2ef0c2ea52d54d01b6b4763cc1a99c11
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06919361B2
Reaction notes
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