Acetic acid, (2-benzothiazolylamino)oxo- → 2-Amino-4-methoxy-7-phenyl-benzothiazole
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[S:16]1C2C=CC=CC=2[N:18]=[C:17]1NC(=O)C(O)=O>>[NH2:18][C:17]1[S:16][C:3]2[C:4]([C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][CH:15]=3)=[CH:5][CH:6]=[C:7]([O:8][CH3:9])[C:2]=2[N:1]=1Participants
3
Procedure
The title compound was prepared from 3-amino-4-methoxy-biphenyl, according to the patent literature N-(Benzothiazol-2-yl)oxamic acid derivatives. W. Winter, M. Thiel, A. Roesch and O. H. Wilhelms, German Patent, DE 2656468, 1978. and is obtained as a white solid, MS: m/e=256 (M+), mp. 207-208° C.
Workup
- customand is obtained as a white solid, MS
Sources & evidence
- ORD record
- ord-84a3c124e2ba4f36afd7c8ad255df978
- Source dataset
- uspto-grants-2008_01
- Patent number
- US07317007B2
Reaction notes
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