تفاعل #42344
ord-d945e176239c4c6c9e6013b66b49819e
معادلة التفاعل
المتفاعلات
الكواشف
ظروف التفاعل
المعالجة
- 1درجة الحرارةThe reaction mixture is heated
- 2درجة الحرارةat reflux for 2 h
- 3درجة الحرارةThe reaction mixture is cooled
- 4غسيلwashed with water, and brine
- 5تجفيفdried (sodium sulfate)
- 6ترشيحfiltered
- 7تركيزconcentrated under reduced pressure
- 8أخرىPurification by flash column chromatography (silica gel, 60% ethyl acetate/hexane)
- 9أخرىprovides a solid
- 10workup.ADDITIONis added
- 11غسيلwashed with 1N hydrochloric acid (aq), water, and brine
- 12تجفيفdried (sodium sulfate)
- 13ترشيحfiltered
- 14تركيزconcentrated under reduced pressure
الإجراء التجريبي
To a −70° C. stirred solution of oxazole (330 mg, 4.8 mmol) in tetrahydrofuran (4 mL) is added n-butyllithium (1.6 M in hexanes, 3.3 mL, 5.3 mmol). After 30 min, zinc chloride (1 M in diethyl ether, 14.5 mL, 14.5 mmol) is added and the reaction mixture is warmed to 0° C. for 1 h. To this mixture is added a solution of methyl 3-iodo-5-{[methyl(propyl)amino]carbonyl}benzoate (1.6 g, 4.5 mmol) in anhydrous tetrahydrofuran (3 mL) followed by palladium(0)tetrakis(triphenylphosphine) (221 mg, 0.19 mmol). The reaction mixture is heated at reflux for 2 h. The reaction mixture is cooled, diluted with ethyl acetate, washed with water, and brine, dried (sodium sulfate), filtered, and concentrated under reduced pressure. Purification by flash column chromatography (silica gel, 60% ethyl acetate/hexane) provides a solid. The solid is redissolved in 1:1:1 tetrahydrofuran/methanol/water (9 mL), and lithium hydroxide monohydrate (311 mg, 7.4 mmol) is added and stirred 2 h at room temperature. The reaction is diluted in chloroform and washed with 1N hydrochloric acid (aq), water, and brine, dried (sodium sulfate), filtered and concentrated under reduced pressure to give the title compound. ESI MS m/z 287.3 [M−H]−.