反応 #56891

反応方程式

sodium chloride

hydrochloric acid

4-{4-[2-amino-6-(5-chloro-2-ethoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-butyric acid ethyl ester

sodium hydroxide

→

title compound

収率 66.0%

4-{4-[2-Amino-6-(5-chloro-2-ethoxy-phenyl)-pyrimidin4-ylamino]-phenyl}-butyric acid

収率 66.0%

溶媒

Ethyl acetate

ethanol

反応条件

後処理

1. 1
   workup.STIRRINGthe mixture was stirred for 10 minutes
2. 2
   濃縮The organic layer was concentrated under reduced pressure
3. 3
   workup.ADDITIONThe residual solid was treated with water (25 ml)
4. 4
   workup.STIRRINGstirred vigorously
5. 5
   ろ過Suction filtration

実験手順

A mixture of 4-{4-[2-amino-6-(5-chloro-2-ethoxy-phenyl)-pyrimidin-4-ylamino]-phenyl}-butyric acid ethyl ester (350 mg, 0.71 mmol), sodium hydroxide (150 mg, 3.8 mmol) and ethanol (5 ml) was stirred for 18 hours. Ethyl acetate (100 ml), saturated aqueous sodium chloride solution (100 ml) and concentrated hydrochloric acid (1 ml) were added and the mixture was stirred for 10 minutes. The organic layer was concentrated under reduced pressure. The residual solid was treated with water (25 ml) and stirred vigorously. Suction filtration afforded the title compound (200 mg 61% yield) as a white powder. 1H NMR (DMSO-d6) δ 1.38 (m, 3H, CH3), 1.83 (m, 2H, CH2), 2.23 (m, 2H, CH2), 2.61 (m, 2H, CH2), 4.17 (m, 2H, CH2), 6.60 (s, 1H, Ar), 7.20-7.29 (m, 3H, Ar), 7.61-7.71 (m, 4H, Ar), 10.76 (s, 1H, NH), 12.48 (s, 1H).

出典