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ChemicalBook CAS DataBase List Gefitinib InterMediate B
912556-91-3

Gefitinib InterMediate B synthesis

13synthesis methods
1-Bromo-3-chloropropane

109-70-6

O-Desmorpholinopropyl Gefitinib

184475-71-6

Gefitinib InterMediate B

912556-91-3

A mixture of 4-((3-chloro-4-fluorophenyl)amino)-7-methoxyquinazolin-6-ol (20.00 g), K2CO3 (10.37 g), KI (1.04 g), 1-bromo-3-chloropropane (7.50 mL), and DMF (150 mL) was stirred and reacted for 6 hours at 40 °C. After completion of the reaction, the reaction mixture was poured into water and the solid was collected by filtration. The filtrate was purified by silica gel column chromatography (eluent: ethyl acetate) to afford the target compound, N-(3-chloro-4-fluorophenyl)-6-(3-chloropropoxy)-7-methoxyquinazolin-4-amine, as a light yellow liquid (22.05 g, 89.00% yield). The structure of the compound was confirmed by the following spectral data: mass spectrum (ESI, positive ion mode) m/z: 396.1 ([M+H]+); 1H NMR (400 MHz, CDCl3) δ: 2.01 (m, 2H), 3.68 (t, J=4.2 Hz, 2H), 4.00 (s, 3H), 4.10 (t, J=4.2 Hz, 2H). 6.80 (s, 1H), 7.16 (s, 1H), 7.26 (s, 1H), 7.30 (s, 1H), 7.47 (s, 1H), 8.64 (s, 1H) ppm.

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Yield:912556-91-3 93%

Reaction Conditions:

in isopropyl alcohol; for 3 h;Heating;

References:

Ming, Dong Li;You, Guang Zheng;Ji, Min [Molecules,2007,vol. 12,# 3,p. 673 - 678]

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