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[ CAS No. 161563-79-7 ] {[proInfo.proName]}

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Chemical Structure| 161563-79-7
Chemical Structure| 161563-79-7
Structure of 161563-79-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 161563-79-7 ]

CAS No. :161563-79-7 MDL No. :MFCD03086213
Formula : C7H8N4OS Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 196.23 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 161563-79-7 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 161563-79-7 ]

[ 161563-79-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 57626-37-6 ]
  • [ 161563-79-7 ]
YieldReaction ConditionsOperation in experiment
89% With hydrazine hydrate; In ethanol; for 3h;Reflux; To the stirred solution of <strong>[57626-37-6]ethyl 6-methylimidazo[2,1-b]thiazole-5-carboxylate</strong> (2a) (5.20 g) in ethanol (40 mL) was added 35%aqueous solution of N2H4H2O (40 mL) and refluxed for 3 h. Thereaction mixture was concentrated to half volume and cooled onice bath, the solids formed were filtered and dried in vacuum ovento get 6-methylimidazo[2,1-b]thiazole-5-carbohydrazide (3a)(4.30 g, 89%) as an Off-white solid. ESI-MS showed 197 [M+H]+.
  • 2
  • [ 2215-77-2 ]
  • [ 161563-79-7 ]
  • 6-methyl-N'-(4-phenoxybenzoyl)imidazo[2,1-b]thiazole-5-carbohydrazide [ No CAS ]
YieldReaction ConditionsOperation in experiment
88% Stage #1: 4-Phenoxybenzoic acid With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine In dichloromethane at 0℃; Stage #2: 6-methylimidazo-<2,1-b>thiazole-5-carbohydrazide In dichloromethane at 20℃; for 3h; 10 4.1.7. General procedure for the synthesis of final molecules(5aa-ae and 5ba-be) General procedure: To the stirred solution of R-COOH (1.0 equiv), in CH2Cl2 at 0 Cwas added EDCI (1.2 equiv), HOBt (1.2 equiv) and Et3N (2.0 equiv)stirred for few minutes then was added 6-methylimidazo[2,1-b]thiazole-5-carbohydrazide (for 5aa-ae)/2-methylbenzo[d]imidazo[2,1-b]thiazole-3-carbohydrazide (for 5ba-be) (1.2 equiv), andallowed stir at rt for 3 h, The reaction mixture was diluted withCH2Cl2 and washed with H2O and the separated organic layerwas concentrated under reduced pressure, purified by columnchromatography.
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