Cyanoacetamide → HCID 178509839, compound
Reaction equation
[C:1](CC(N)=O)#[N:2].[OH:7][C:8]1[C:12]([C:13]#[N:14])=[C:11]([NH:15][C:16]2[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=2)[S:10][N:9]=1>>[OH:7][C:8]1[C:12]([C:13]#[N:14])=[C:11]([NH:15][C:16]2[CH:17]=[CH:18][CH:19]=[C:20]([C:1]#[N:2])[CH:21]=2)[S:10][N:9]=1Participants
3
Procedure
The title compound was prepared from 1-isothiacyanato-3-cyano-benzene and 2-cyanoacetamide by the procedure analogous to Method 2 for 3-Hydroxy-5-phenylamino-isothiazol-4-carbonitrile. 1H NMR (CD3OD) δ: 7.5–7.7 (m, 4H) ppm; MS (ES, m/z): 242.9, [M-H]+, 241.1 [M-H]−.
Sources & evidence
- ORD record
- ord-a4e05381d3e4404b89d0cc5266d70a11
- Source dataset
- uspto-grants-2006_01
- Patent number
- US06989451B2
Reaction notes
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