Isopropanol → HCID 59753894, compound
Reaction equation
CS([C:5]1[N:10]=[C:9]([O:11][C:12]2[CH:17]=[CH:16][C:15]([F:18])=[C:14]([F:19])[CH:13]=2)[C:8]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)=[C:7]([C:27]2[CH:32]=[CH:31][C:30]([Cl:33])=[CH:29][C:28]=2[Cl:34])[N:6]=1)(=O)=O.C([Li])CCC.[CH:40]([OH:43])([CH3:42])[CH3:41]>>[CH:40]([O:43][C:5]1[N:10]=[C:9]([O:11][C:12]2[CH:17]=[CH:16][C:15]([F:18])=[C:14]([F:19])[CH:13]=2)[C:8]([C:20]2[CH:25]=[CH:24][C:23]([Cl:26])=[CH:22][CH:21]=2)=[C:7]([C:27]2[CH:32]=[CH:31][C:30]([Cl:33])=[CH:29][C:28]=2[Cl:34])[N:6]=1)([CH3:42])[CH3:41]Participants
4
Procedure
2-Methylsulfonyl-4-(3,4-difluorophenoxy)-5-(4-chlorophenyl)-6-(2,4-dichlorophenyl)pyrimidine from Example 20 (30 mg, 0.06 mmol) with 2 equivalents each of n-butyl lithium and isopropyl alcohol by the procedure described in Reference Example 6 and 7 to afford the title compound: HPLC/MS: m/e=521 (M++1); Rt=4.93 min. 1H-NMR 400 MHz (CDCl3): δ 1.33 (d, J=6 Hz, 6H), 5.02-5.09 (m, 1H), 6.90-6.94 (m, 1H), 7.04-7.10 (m, 1H), 7.12-7.28 (m, 7H), 7.35 (d, J=2 Hz, 1H).
Sources & evidence
- ORD record
- ord-1d34d03897f6492ba224aa83f0885a06
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07405221B2
Reaction notes
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