1-Methylpiperazine → 4-(4-Chloro-2-fluoroanilino)-6-methoxy-7-(3-(4-methylpiperazin-1-ylcarbonyl)propoxy)quinazoline

1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (145 mg, 0.75 mmol) was added to a mixture of 7-(3-carboxypropoxy)-4-(4-chloro-2-fluoroanilino)-6-methoxyquinazoline (250 mg, 0.62 mmol), (prepared as described for the starting material in Example 42), 1-methylpiperazine (0.21 ml, 2.32 mmol) and 4-dimethylaminopyridine (300 mg, 2.46 mol) in DMF (7.5 ml). The reaction mixture was stirred at ambient temperature for 24 hours and the volatiles were removed by evaporation. Water was added to the residue and the aqueous mixture was extracted with methylene chloride (3×30 ml). The combined organic extracts were washed with brine and the solvent was removed by evaporation. The residue was triturated with ether and the precipitate was collected by filtration. The solid was purified by column chromatography eluting with methylene chloride/methanol/aqueous ammonia (100/8/1). The purified product was triturated with ether collected by filtration and dried to give 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(3-(4-methylpiperazin-1-ylcarbonyl)propoxy)quinazoline (133 mg, 44%).

1. custom(prepared
2. customthe volatiles were removed by evaporation
3. additionWater was added to the residue
4. extractionthe aqueous mixture was extracted with methylene chloride (3×30 ml)
5. washThe combined organic extracts were washed with brine
6. customthe solvent was removed by evaporation
7. customThe residue was triturated with ether
8. filtrationthe precipitate was collected by filtration
9. customThe solid was purified by column chromatography
10. washeluting with methylene chloride/methanol/aqueous ammonia (100/8/1)
11. customThe purified product was triturated with ether
12. filtrationcollected by filtration
13. customdried

ORD record

ord-504815f5d85d411281b717570eafaf68

Source dataset

uspto-grants-2004_01

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06673803B2