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Chemical Structure| 1216142-18-5 Chemical Structure| 1216142-18-5

Structure of 1216142-18-5

Chemical Structure| 1216142-18-5

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Product Details of [ 1216142-18-5 ]

CAS No. :1216142-18-5
Formula : C10H9ClN2O2
M.W : 224.64
SMILES Code : O=C(C1=C(CC)N=C2C=CC(Cl)=CN21)O
MDL No. :MFCD14551378

Safety of [ 1216142-18-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 1216142-18-5 ]

* 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 [ 1216142-18-5 ]

[ 1216142-18-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 852180-47-3 ]
  • [ 1216142-18-5 ]
  • C26H32ClN5O3 [ No CAS ]
YieldReaction ConditionsOperation in experiment
47% With benzotriazol-1-ol; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; triethylamine; In tetrahydrofuran; at 20℃; for 16h; A mixture of compound 6-chloro-2-ethylimidazo[1,2-a]pyridine-3-carboxylic acid (140 mg, 0.48 mmol), G2 (90 mg, 0.40 mmol), EDCI (234 mg, 1.20 mmol), HOBt (162 mg, 1.20 mmol) and TEA (121 mg, 2.00 mmol) in THF (10 mL) was stirred at 20 C for 16 hours. LCMS showed the reaction was finished. The reaction mixture was poured into water (30 mL), extracted with EtOAc (20 mL X 3). The combined extracts were washed with brine (10 mL), dried over anliydrous Na2SO4 and concentrated to give a residue. The residue was purified by silica gel column (eluent: PE/EtOAc = 8/1 to 4/1) to afford 120 mg (yield: 47%) of compound G3 as a white powder.
 

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