| Identification | Back Directory | [Name]
4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine | [CAS]
570407-42-0 | [Synonyms]
Avatrombopag Impurity 13
2-Thiazolamine, 4-(4-chloro-2-thienyl)-5-(4-cyclohexyl-1-piperazinyl)-
4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine
5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine4-(4-chlorothiophen-2-yl)- | [Molecular Formula]
C17H23ClN4S2 | [MDL Number]
MFCD32709643 | [MOL File]
570407-42-0.mol | [Molecular Weight]
382.97 |
| Chemical Properties | Back Directory | [Boiling point ]
560.0±50.0 °C(Predicted) | [density ]
1.345±0.06 g/cm3(Predicted) | [pka]
7.58±0.70(Predicted) | [InChI]
InChI=1S/C17H23ClN4S2/c18-12-10-14(23-11-12)15-16(24-17(19)20-15)22-8-6-21(7-9-22)13-4-2-1-3-5-13/h10-11,13H,1-9H2,(H2,19,20) | [InChIKey]
FQQOPZRSAIEOGH-UHFFFAOYSA-N | [SMILES]
S1C(N2CCN(C3CCCCC3)CC2)=C(C2SC=C(Cl)C=2)N=C1N |
| Hazard Information | Back Directory | [Uses]
4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine is a valuable organic compound that could be used as an intermediate to synthesize thrombopoietin | [Application]
Avatrombopag Maleate | [Synthesis]
4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine is synthesize from the reacton of 4- (4-Chloro-2-thienyl) -5-bromo-2-thiazolylamine with cyclohexylpiperazine. The reaction mixture was extracted with water and EtOAc. The combined organic phases were washed with distilled water and brine and dried to afford 4-(4-chlorothiophen-2-yl)-5-(4-cyclohexylpiperazin-1-yl)thiazol-2-amine.
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