HCID 23030470, compound → 6-Iodoquinazolin-4-one
Reaction equation
[I:1][C:2]1[CH:10]=[C:6]([C:7]([O-])=[O:8])[C:5]([NH2:11])=[CH:4][CH:3]=1.[NH4+:12].[CH:13]([O-])([O-])OC>CO>[I:1][C:2]1[CH:10]=[C:6]2[C:5](=[CH:4][CH:3]=1)[N:11]=[CH:13][NH:12][C:7]2=[O:8]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
In a 2-mL volume stainless steel pressure-resistant vessel were placed 530 mg (1.9 mmol) of ammonium 5-iodoanthranilate (prepared in the same manner as in Reference Example 4), 403 mg (3.8 mmol) of methyl orthoformate, and 1.5 mL of methanol. The reaction was carried out at 120° C. for 2 hours. After the reaction was complete, the reaction mixture was cooled to room temperature and analyzed (according to absolute quantitative analysis) by high performance liquid chromatography. There was produced 402 mg (reaction yield: 77%) of 6-iodoquinazolin-4-one.
Workup
- customIn a 2-mL volume stainless steel pressure-resistant vessel were placed
Sources & evidence
- ORD record
- ord-34392f6d71094927894e1692f32feda2
- Source dataset
- uspto-grants-2007_06
- Patent number
- US07232903B2
Reaction notes
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