Hydrochloric Acid → HCID 21090728, compound
Reaction equation
[ClH:1].[CH3:2][O:3][C:4]1[CH:9]=[CH:8][C:7]([N:10]2[C:14]([C:15]3[CH:31]=[CH:30][C:18]([O:19][CH2:20][CH2:21][NH:22]C(=O)OC(C)(C)C)=[CH:17][CH:16]=3)=[CH:13][C:12]([C:32]([F:35])([F:34])[F:33])=[N:11]2)=[CH:6][CH:5]=1>C(OCC)(=O)C>[ClH:1].[CH3:2][O:3][C:4]1[CH:5]=[CH:6][C:7]([N:10]2[C:14]([C:15]3[CH:31]=[CH:30][C:18]([O:19][CH2:20][CH2:21][NH2:22])=[CH:17][CH:16]=3)=[CH:13][C:12]([C:32]([F:35])([F:33])[F:34])=[N:11]2)=[CH:8][CH:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of hydrogen chloride in ethyl acetate (4N, 1.0L) was added powdered tert-Butyl 2-{4-[1-(4-methoxyphenyl)-3-(trifluoromethyl)-1H-pyrazol-5-yl]-phenoxy}ethylcarbamate obtained by Example 73 (500 g) at 5° C. over 20 min.
Workup
- customat 5° C.
- customover 20 min.
Sources & evidence
- ORD record
- ord-0d98bbb04f4046a5b30a9f0ba3e4399f
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07183306B2
Reaction notes
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