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Chemical Structure| 911417-24-8 Chemical Structure| 911417-24-8

Structure of 911417-24-8

Chemical Structure| 911417-24-8

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Product Details of [ 911417-24-8 ]

CAS No. :911417-24-8
Formula : C16H11ClN2O2
M.W : 298.72
SMILES Code : CC(OC1=CC=CC(C2=NC(Cl)=C3C=CC=CC3=N2)=C1)=O
MDL No. :MFCD28167877

Safety of [ 911417-24-8 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 911417-24-8 ]

* 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 [ 911417-24-8 ]

[ 911417-24-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 129488-10-4 ]
  • [ 911417-24-8 ]
  • [ 911417-25-9 ]
YieldReaction ConditionsOperation in experiment
98% In isopropyl alcohol; at 95℃; for 0.25h; 3-(4-Chloroquinazolin-2-yl)phenyl acetate (9.77 g, 29.97mmole) was dissolved in isopropanol (290 mL) and tert-butyl 5-amino-lH-indazole-l-carboxylate (6.99 g, 29.97 mmole) was added. The solution was heated to 95 0C and stirred for 0.25 h. A gelatinous formation developed which was manually broken up and dissolution gradually occurred followed by formation of a yellow precipitate. The reaction was stirred for an additional EPO <DP n="108"/>0.25 h, cooled to ambient temperature and filtered. The filtered solid was washed with ether and then dried under high vacuum overnight to give tert-butyl 5-(2-(3- acetoxyphenyl)quinazolin-4-ylamino)-lH-indazole-l-carboxylate. (14.58 g, mmol, 98 percent)
98% In isopropyl alcohol; at 95℃; for 0.5h; 3-(4-ChIoroquinazolin-2-yl)phenyl acetate (9.77 g, 29.97mmole) was dissolved in isopropanol (290 mL) and /m-butyl 5-amino- I H-indazole-l -carboxylate (6.99 g, 29.97 mmole) was added. The solution was heated to 95 °C and stirred for 0.25 h. A gelatinous formation developed which was manually broken up and dissolution gradually occurred followed by formation of a yellow precipitate. The reaction was stirred for an additional 0.25 h, cupsilonupsilonled lupsilon ambient temperature and Tillered. The filtered solid was washed wilh ether and then dried under high vacuum overnight to give ten-butyl 5-(2-(3- acetoxyphenyl)quinazolin-4-ylamino)- I H-indazole- l -carboxylate. ( 14.58 g, mmol, 98 percent)
98% In isopropyl alcohol; at 95℃; for 0.5h; [0181] 3-(4-Chloroquinazolin-2-yl)phenyl acetate (9.77 g, 29.97mmole) was dissolved in isopropanol (290 mL) and tert-butyl 5-amino-lH-indazole-l-carboxylate (6.99 g, 29.97 mmole) was added. The solution was heated to 95 0C and stirred for 0.25 h. A gelatinous formation developed which was manually broken up and dissolution gradually occurred followed by formation of a yellow precipitate. The reaction was stirred for an additional 0.25 h, cooled to ambient temperature and filtered. The filtered solid was washed with ether and then dried under high vacuum overnight to give tert-butyl 5-(2-(3- acetoxyphenyl)quinazolin-4-ylamino)-lH-indazole-l-carboxylate. (14.58 g, mmol, 98 percent)
 

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