4-Methoxy-2,3,6-trimethylbenzenesulfonyl chloride → HCID 10258514, compound
Reaction equation
[NH2:1][C:2]1[CH:31]=[CH:30][C:5]([CH2:6][C:7]2[NH:15][C:14]3[C:13](=[O:16])[N:12]([CH2:17][C:18]4[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=4[F:24])[C:11](=[O:25])[N:10]([CH2:26][CH2:27][CH2:28][CH3:29])[C:9]=3[N:8]=2)=[CH:4][CH:3]=1.[CH3:32][O:33][C:34]1[CH:39]=[C:38]([CH3:40])[C:37]([S:41](Cl)(=[O:43])=[O:42])=[C:36]([CH3:45])[C:35]=1[CH3:46]>>[CH2:26]([N:10]1[C:9]2[N:8]=[C:7]([CH2:6][C:5]3[CH:4]=[CH:3][C:2]([NH:1][S:41]([C:37]4[C:38]([CH3:40])=[CH:39][C:34]([O:33][CH3:32])=[C:35]([CH3:46])[C:36]=4[CH3:45])(=[O:43])=[O:42])=[CH:31][CH:30]=3)[NH:15][C:14]=2[C:13](=[O:16])[N:12]([CH2:17][C:18]2[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=2[F:24])[C:11]1=[O:25])[CH2:27][CH2:28][CH3:29]Participants
3
Procedure
Prepared from 8-(4-amino-benzyl)-3-butyl-1-(2-fluoro-benzyl)-3,7-dihydro-purine-2,6-dione and 4-methoxy-2,3,6-trimethyl-benzenesulfonyl chloride. Purity (ELSD, based on MW=633.7)=80%.
Sources & evidence
- ORD record
- ord-dc70df3ff41f400097f3e82dc7487660
- Source dataset
- uspto-grants-2006_12
- Patent number
- US07148229B2
Reaction notes
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