2-Methylaziridine → HCID 58808774, compound
Reaction equation
[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[O:15][C:14]([C:16]([OH:18])=O)=[CH:13][CH:12]=2)[CH:4]=1)[CH3:2].[CH3:19][CH:20]1[CH2:22][NH:21]1>>[CH2:1]([C:3]1[C:8](=[O:9])[NH:7][C:6]([CH3:10])=[C:5]([C:11]2[O:15][C:14]([C:16]([N:21]3[CH2:22][CH:20]3[CH3:19])=[O:18])=[CH:13][CH:12]=2)[CH:4]=1)[CH3:2]Participants
3
Procedure
Method 1, Example 205 is substantially repeated except for utilizing 5-(5-ethyl-2-methyl-6-oxo-1,6-dihydropyridin-3-yl)furan-2-carboxylic acid and 2-methylaziridine to give the title compound (81% yield). LC/MS: RT 2.02 min; m/e 287 (M+H).
Sources & evidence
- ORD record
- ord-b8f7ca5f248b49bfa628633ea955d4b7
- Source dataset
- uspto-grants-2012_05
- Patent number
- US08173682B2
Reaction notes
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