4-Methoxy-7-morpholinobenzo[d]thiazol-2-amine → HCID 11633373, compound
Reaction equation
[CH3:1][O:2][C:3]1[C:8]2[N:9]=[C:10]([NH2:12])[S:11][C:7]=2[C:6]([N:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)=[CH:5][CH:4]=1.C1([O:25][C:26]([C:28]2[CH:29]=[N:30][N:31]([CH2:33][CH2:34][N:35]([CH3:37])[CH3:36])[CH:32]=2)=O)C=CC=CC=1>>[CH3:1][O:2][C:3]1[C:8]2[N:9]=[C:10]([NH:12][C:26]([C:28]3[CH:29]=[N:30][N:31]([CH2:33][CH2:34][N:35]([CH3:37])[CH3:36])[CH:32]=3)=[O:25])[S:11][C:7]=2[C:6]([N:13]2[CH2:18][CH2:17][O:16][CH2:15][CH2:14]2)=[CH:5][CH:4]=1Participants
3
Procedure
Using 4-methoxy-7-morpholin-4-yl-benzothiazol-2-ylamine and 1-(2-dimethylamino-ethyl)-1H-pyrazole-4-carboxylic acid phenyl ester, the title compound was obtained as white crystals 54% yield). MS: m/e=431(M+H+), mp 203-205° C.
Sources & evidence
- ORD record
- ord-2f45c4288cf84910bfe5574166d09a63
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07371749B2
Reaction notes
Loading…