4-Methoxy-7-morpholinobenzo[d]thiazol-2-amine → HCID 11676060, compound

HRID 2222090Notes

Reaction equation

HRID 2222090 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][O:35][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][O:35][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]=1

Participants

3

Reactant 2

HCID 114028614-Methoxy-7-morpholinobenzo[d]thiazol-2-amineHCID 58592595HCID 58592595, compound

Product 1

HCID 11676060HCID 11676060, compound

Procedure

Using 4-methoxy-7-morpholin-4-yl-benzothiazol-2-ylamine and 1-(2-methoxy-ethyl)-1H-pyrazole-4-carboxylic acid phenyl ester, the title compound was obtained as light yellow crystals 43% yield). MS: m/e=418(M+H+), mp 191-193° C.

Sources & evidence

ORD record
ord-4be6493948c3418a99aeb8ff4c138dc1
Source dataset
uspto-grants-2008_05
Patent number
US07371749B2

Reaction notes

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