Triphenylphosphine → 4-(4-Chloro-2-fluoroanilino)6-methoxy-7-(2-(3-oxomorpholino)ethoxy)quinazoline hydrochloride

Diethyl azodicarboxylate (400 mg, 2.3 mmol) was added dropwise to a mixture of 4-(4-chloro-2-fluoroanilino)-7-hydroxy-6-methoxyquinazoline (250 mg, 0.78 mmol), (prepared as described for the starting material in Example 2), triphenylphosphine (615 mg, 2.3 mmol) and 4-(2-hydroxyethyl)-3-morpholinone (170 mg, 1.17 mmol), (EP 580402A2), in methylene chloride (5 ml) under nitrogen. The mixture was stirred for 4 hours at ambient temperature, methylene chloride (5 ml) was added and stirring was continued for a further 18 hours at ambient temperature. THF (5 ml). 4-(2-hydroxyethyl)-3-morpholinone (113 mg, 0.78 mmol). triphenylphosphine (204 mg, 0.78 mmol) were added and diethyl azodicarboxylate (136 mg, 0.78 mmol) was then added dropwise. The mixture was stirred for 5 minutes at ambient temperature, and was purified by pouring directly onto a silica column, eluting with methylene chloride/ethyl acetate/methanol (5/4/1). The purified solid was dissolved in methylene chloride and 2M methanolic hydrogen chloride (0.5 ml) was added. The mixture was concentrated by evaporation and then diluted with ether. The resulting precipitate was collected by filtration, washed with ether and dried under vacuum to give 4-(4-chloro-2-fluoroanilino)-6-methoxy-7-(2-(3-oxomorpholino)ethoxy)quinazoline hydrochloride (150 mg, 39%).

1. custom(prepared
2. stirringstirring
3. waitwas continued for a further 18 hours at ambient temperature
4. stirringThe mixture was stirred for 5 minutes at ambient temperature
5. customwas purified
6. additionby pouring directly onto a silica column
7. washeluting with methylene chloride/ethyl acetate/methanol (5/4/1)
8. dissolutionThe purified solid was dissolved in methylene chloride
9. addition2M methanolic hydrogen chloride (0.5 ml) was added
10. concentrationThe mixture was concentrated by evaporation
11. additiondiluted with ether
12. filtrationThe resulting precipitate was collected by filtration
13. washwashed with ether
14. customdried under vacuum

ORDレコード

ord-b365bb33fed046b29e4ffb3582cf0fd6

出典データセット

uspto-grants-2011_05

DOI

10.6084/m9.figshare.5104873.v1

特許番号

USRE042353E1