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Chemical Structure| 1172851-61-4 Chemical Structure| 1172851-61-4

Structure of 1172851-61-4

Chemical Structure| 1172851-61-4

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Product Details of [ 1172851-61-4 ]

CAS No. :1172851-61-4
Formula : C9H6ClIN2O
M.W : 320.51
SMILES Code : COC1=CC2=NC=NC(Cl)=C2C=C1I
MDL No. :MFCD12973651
InChI Key :VGUHUPXWUUVYHC-UHFFFAOYSA-N
Pubchem ID :76848204

Safety of [ 1172851-61-4 ]

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

Application In Synthesis of [ 1172851-61-4 ]

* 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 [ 1172851-61-4 ]

[ 1172851-61-4 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 1123-93-9 ]
  • [ 1172851-61-4 ]
  • N-(1,3-benzothiazol-5-yl)-6-iodo-7-(methyloxy)-4-quinazolinamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
93% In isopropyl alcohol; at 90℃; for 0.5h; To asolution of 4-chloro-6-iodo-7-(methyloxy)quinazoline (2.0 g, 5.4 mmol) in isopropanol (3030 mL) was added <strong>[1123-93-9]1,3-benzothiazol-5-amine</strong> (1.2 g, 8.1 mmol). The suspension was heated inoil bath at 90C (preheated). The reaction mixture stirred at this temperature for 30 min.A yellow solid precipitated out as the reaction mixture was allowed to cool to rt. The solid-was filtered to provide 2.1 g of the title compound (77%, 93% pure). MS: m/z: 471[M+H+]
55.2% In propan-1-ol; at 90℃; for 0.5h; Step 5. N-l,3-benzothiazol-5-yl-6-iodo-7-(methyloxy)-4-quinazolinamine: To a solution of 4-chloro-6-iodo-7-(methyloxy)quinazoline (2.0 g, 5.4 mmol) in 1-propanol (30 mL) was added l,3-benzothiazol-5-amine (1.2 g, 8.1 mmol). The suspension was heated in oil bath at 90C (preheated). The reaction mixture was stirred at this temperature for 30 min. A yellow solid precipitated out as the reaction mixture was allowed to cool to rt. The solid was filtered, washed with toluene and dried to provide 1.3g of the title compound (55.2%, 99% pure). MS: m/z: 435 [M+H]+.
In isopropyl alcohol; at 90℃; for 0.5h; To a solution of 4-chloro-6-iodo-7-(methyloxy)quinazoline (2.0 g, 5.4 mmol) in isopropanol (30 mL) was added <strong>[1123-93-9]1,3-benzothiazol-5-amine</strong> (1.2 g, 8.1 mmol). The suspension was heated in oil bath at 90C (preheated). The reaction mixture stirred at this temperature for 30 min. A yellow solid precipitated out as the reaction mixture was allowed to cool to rt. The solid was filtered to provide 2.1 g of the title compound (77%, 93% pure). MS: m/z: 471 [M+H]+.
 

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Related Functional Groups of
[ 1172851-61-4 ]

Chlorides

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Related Parent Nucleus of
[ 1172851-61-4 ]

Quinazolines

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