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Chemical Structure| 136549-13-8 Chemical Structure| 136549-13-8

Structure of 136549-13-8

Chemical Structure| 136549-13-8

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Product Details of [ 136549-13-8 ]

CAS No. :136549-13-8
Formula : C8H8ClN3
M.W : 181.62
SMILES Code : CC1=NN2C(=C1)N=C(C)C=C2Cl
MDL No. :MFCD11043774
InChI Key :QGROGNQUPBOMJQ-UHFFFAOYSA-N
Pubchem ID :18406987

Safety of [ 136549-13-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of [ 136549-13-8 ]

* 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 [ 136549-13-8 ]

[ 136549-13-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 136549-13-8 ]
  • [ 16803-92-2 ]
  • N-(4-chlorophenyl)-4-((2,5-dimethylpyrazolo[1,5-a]pyrimidin-7-yl)amino)benzenesulfonamide hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
25% General procedure: A mixture of 0.001 mol of compound (41a-d or 45), 1 equivalentof the respective 4-amino-N-arylbenzenesulfonamides (44a-g) and3 mL of ethanol was stirred and refluxed (78 C) for 2 h. The reactionmixture was poured into ice water, and the precipitateformed was vacuum filtered and washed with water. The precipitatewas purified by recrystallization from methanol/water (2:1) orchromatography TLC Glass Plates (Merck TLC Silica gel 60 RP-18F254s) in chloroform/methanol (9.5:0.5). After purification, therespective hydrochloride was prepared, and the molecules weresolubilized and stirred for 15 min in a 1:1 solution of HCl/H2O andconcentrated under vacuum [17e19].
 

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Related Functional Groups of
[ 136549-13-8 ]

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Related Parent Nucleus of
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