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Chemical Structure| 121952-97-4 Chemical Structure| 121952-97-4

Structure of 121952-97-4

Chemical Structure| 121952-97-4

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Product Details of [ 121952-97-4 ]

CAS No. :121952-97-4
Formula : C10H10N2S
M.W : 190.27
SMILES Code : NC1=NC=C(CC2=CC=CC=C2)S1
MDL No. :MFCD00547831

Safety of [ 121952-97-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P264-P302+P352-P304+P340-P305+P351+P338-P332+P313-P337+P313

Application In Synthesis of [ 121952-97-4 ]

* 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 [ 121952-97-4 ]

[ 121952-97-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 68947-43-3 ]
  • [ 121952-97-4 ]
  • N-(5-benzylthiazol-2-yl)-1-methylpiperidine-4-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
20% With dmap; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In dichloromethane; N,N-dimethyl-formamide; at 20℃; for 2h;Inert atmosphere; General procedure: To a mixture of compound 3a (1equiv), alicyclic carboxylic acid (1.3equiv), DMAP (0.45equiv), triethylamine (1.8equiv) in DCM/DMF (?2mL 3:1, v:v) was added EDAC (1.8equiv) at room temperature. The reaction mixture was stirred for 2h, diluted with EtOAc, and washed with brine, aqueous HCl (0.2N), and aqueous sodium bicarbonate solution. The organic phase was dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by silica gel column chromatography.
  • 2
  • [ 127116-19-2 ]
  • [ 121952-97-4 ]
  • 2-(4-(6-((5-benzylthiazol-2-yl)amino)-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanol [ No CAS ]
 

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