3,5-Dimethyl-4-methoxybenzoyl chloride → HCID 178489873, compound
Reaction equation
[CH3:1][S:2][C:3]1[N:4]=[C:5]([OH:19])[C:6]2[N:11]=C(C3C=CC=C(C)C=3)O[C:7]=2[N:8]=1.[CH3:20][O:21][C:22]1[C:30]([CH3:31])=[CH:29][C:25]([C:26](Cl)=[O:27])=[CH:24][C:23]=1[CH3:32]>>[CH3:20][O:21][C:22]1[C:30]([CH3:31])=[CH:29][C:25]([C:26]2[O:27][C:7]3[N:8]=[C:3]([S:2][CH3:1])[N:4]=[C:5]([OH:19])[C:6]=3[N:11]=2)=[CH:24][C:23]=1[CH3:32]Participants
3
Procedure
2-(4-Methoxy-3,5-dimethyl-phenyl)-5-methylsulfanyl-oxazolo[5,4-d]pyrimidin-7-ol was prepared according to the procedure described in example 1, steps (a) to (d), using 4-methoxy-3,5-dimethylbenzoyl chloride in step (a).
Sources & evidence
- ORD record
- ord-793cb71050dd40e9a40353a6ba325bdc
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08785439B2
Reaction notes
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