Dimethylformamide dimethyl acetal → HCID 18507677, compound
Reaction equation
[CH3:1][O:2][C:3]1[CH:4]=[C:5]([CH:11]=[C:12]([O:16][CH3:17])[C:13]=1[O:14][CH3:15])[C:6]([CH2:8][C:9]#[N:10])=O.COC(OC)[N:21]([CH3:23])C.C(=O)(O)O.[NH2:30][C:31](N)=[NH:32].C[O-].[Na+]>CO>[NH2:32][C:31]1[N:30]=[C:6]([C:5]2[CH:4]=[C:3]([O:2][CH3:1])[C:13]([O:14][CH3:15])=[C:12]([O:16][CH3:17])[CH:11]=2)[C:8]([C:23]#[N:21])=[CH:9][N:10]=1Participants
6
Procedure
From 3,4,5-trimethoxybenzoylacetonitrile and N,N-dimethylformamide dimethyl acetal. Then treatment with guanidine carbonate and sodium methylate in methanol. EI-MS m/e (%): 286 (M+, 100), 271 ([M—CH3]+, 44), 243 (27), 228 (15), 213 (30), 157 (16).
Sources & evidence
- ORD record
- ord-3d513dd741d64d789929f29c35cad1b0
- Source dataset
- uspto-grants-2003_07
- Patent number
- US06586441B2
Reaction notes
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