ChemicalBook--->CAS DataBase List--->788136-89-0

788136-89-0

788136-89-0 Structure

788136-89-0 Structure
IdentificationBack Directory
[Name]

4-(3-Chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-yl acetate
[CAS]

788136-89-0
[Synonyms]

Gefitinib IMpurity VIII
Gefitinib Intermediate 6
Gefitinib interMediate VI
4-((3-Chloro-4-fluorophenyl)
-7-methoxyquinazolin-6-yl acetate
O-Desmorpholinopropyl Gefitinib Acetate
4-(3-Chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-yl ac...
4-(3-Chloro-4-fluorophenylamino)-7-methoxyquizolin-6-yl acetate
4-(3-Chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-yl acetate
4-[(3-Chloro-4-fluorophenyl)amino]-7-methoxy-6-quinazolinol 6-acetate
6-Quinazolinol,4-[(3-chloro-4-fluorophenyl)amino]-7-methoxy-, 6-aceta
6-Quinazolinol,4-[(3-chloro-4-fluorophenyl)amino]-7-methoxy-, 6-acetate
acetic acid [4-(3-chloro-4-fluoroanilino)-7-methoxy-6-quinazolinyl] ester
[Molecular Formula]

C17H13ClFN3O3
[MDL Number]

MFCD11618121
[MOL File]

788136-89-0.mol
[Molecular Weight]

361.75
Chemical PropertiesBack Directory
[Boiling point ]

471.5±45.0 °C(Predicted)
[density ]

1.425
[storage temp. ]

under inert gas (nitrogen or Argon) at 2–8 °C
[pka]

5.22±0.30(Predicted)
Safety DataBack Directory
[Symbol(GHS) ]


GHS07
[Signal word ]

Warning
[Hazard statements ]

H315-H335-H302-H319
[Precautionary statements ]

P264-P280-P305+P351+P338-P337+P313P-P264-P280-P302+P352-P321-P332+P313-P362-P264-P270-P301+P312-P330-P501
Hazard InformationBack Directory
[Uses]

4-((3-Chloro-4-fluorophenyl)amino)-7-methoxyquinazolin-6-yl Acetate, is an impurity of Gefitinib (G304000), an antineoplastic.
[Synthesis]

3-Chloro-4-fluoroaniline

367-21-5

6-Acetoxy-4-chloro-7-methoxyquinazoline

230955-75-6

4-(3-Chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-yl acetate

788136-89-0

General procedure for the synthesis of 4-(3-chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-ol acetate from 3-chloro-4-fluoroaniline and 6-acetoxy-4-chloro-7-methoxyquinazoline: at 65°C, AuCl (4.2 g, 18 mmol), 6-acetoxy-4-chloro-7-methoxyquinazoline (12.6 g, 50 mmol) and 3-chloro-4-fluoroaniline (12.3 g, 85 mmol) were dissolved in 50 mL of methanol for substitution reaction. After completion of the reaction, the reaction mixture was filtered. The filtrate was concentrated and washed with petroleum ether to afford 16.9 g of the intermediate 4-(3-chloro-4-fluorophenylamino)-7-methoxyquinazolin-6-ol acetate in 93.4% yield and 99.91% purity.

[References]

[1] Bioorganic and Medicinal Chemistry, 2010, vol. 18, # 2, p. 870 - 879
[2] Patent: CN105693630, 2016, A. Location in patent: Paragraph 0033
[3] Patent: CN106045980, 2016, A. Location in patent: Paragraph 0024; 0025; 0026
[4] Patent: CN108047209, 2018, A. Location in patent: Paragraph 0041; 0047; 0048
[5] Patent: WO2013/71697, 2013, A1. Location in patent: Paragraph 00195
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