2-Carbamoyloxymethyl-5-isopropyl-1-methyl-4-phenylthio-1H-imidazole → 1H-Imidazole, 5-((3-chlorophenyl)thio)-1,2-dimethyl-4-(1-methylethyl)-
Reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([S:8][C:9]2[NH:13][C:12]([CH3:14])=[N:11][C:10]=2[CH:15]([CH3:17])[CH3:16])[CH:5]=[CH:6][CH:7]=1.[C:18](OCC1N(C)C(C(C)C)=C(SC2C=CC=CC=2)N=1)(=O)N>>[Cl:1][C:2]1[CH:3]=[C:4]([S:8][C:9]2[N:13]([CH3:18])[C:12]([CH3:14])=[N:11][C:10]=2[CH:15]([CH3:17])[CH3:16])[CH:5]=[CH:6][CH:7]=1Participants
3
Procedure
Compound I-3 was obtained from 5-(3-chlorophenylthio)-4-isopropyl-2-methylimidazole by the same synthetic process as that for Compound I-1 in Example 1 (yield 47%). mp 91 to 94° C.
Sources & evidence
- ORD record
- ord-d06ba8ad0d444c548ce855446d614e73
- Source dataset
- uspto-grants-2000_11
- Patent number
- US06147097
Reaction notes
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