Trimethylsilyldiazomethane → HCID 135779826, compound
Reaction equation
[C:1]([C:4]1[NH:13][C:12](=[O:14])[C:11]2[C:6](=[CH:7][C:8]([C:15]([F:18])([F:17])[F:16])=[CH:9][CH:10]=2)[N:5]=1)([CH3:3])=[CH2:2].[Si]([CH:23]=[N+:24]=[N-:25])(C)(C)C>>[CH3:2][C:1]1([C:4]2[NH:13][C:12](=[O:14])[C:11]3[C:6](=[CH:7][C:8]([C:15]([F:17])([F:18])[F:16])=[CH:9][CH:10]=3)[N:5]=2)[CH2:3][CH:23]=[N:24][NH:25]1Participants
3
Procedure
Following the procedure in Example 7, using 2-isopropenyl-7-trifluoromethyl-3H-quinazolin-4-one and TMSCHN2 as starting materials yielded the title compound as a white solid.
Sources & evidence
- ORD record
- ord-7ac8ead4dbe74bebab87ca8db9d7882f
- Source dataset
- uspto-grants-2011_11
- Patent number
- US08053441B2
Reaction notes
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