تفاعل #68625

معادلة التفاعل

1-(3-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)hydrazine

triethylamine

thionyl chloride

2,2-difluoro-2-(3-methoxyquinolin-6-yl)acetic acid

→

2,2-difluoro-N′-(3-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-2-(3-methoxyquinolin-6-yl)acetohydrazide

المردود 33.1%

المذيبات

CH2Cl2

MeOH

CH2Cl2

DMF

ظروف التفاعل

المعالجة

1. 1
   workup.ADDITIONwas added
2. 2
   workup.ADDITIONboth added as solids
3. 3
   درجة الحرارةto warm to rt
4. 4
   workup.STIRRINGstir for 18 h
5. 5
   أخرىThe mixture was quenched with saturated aqueous NaHCO3 (50 mL)
6. 6
   استخلاصthe resulting mixture was extracted with CH2Cl2 (3×50 mL)
7. 7
   تركيزThe combined organic layers were concentrated
8. 8
   درجة الحرارة(heating to 50° C.)
9. 9
   أخرىthe residue purified by SiO2 chromatography solvent system

الإجراء التجريبي

A round bottom flask was charged with 2,2-difluoro-2-(3-methoxyquinolin-6-yl)acetic acid (389 mg, 1536 μmol) and DMF (8 mL). The solution was cooled to 0 C, thionyl chloride (224 μl, 3073 mmol), was added and the resulting solution was maintained 1 h at 0° C. Then, triethylamine (641 μl , 4609 μmol) was added via syringe, followed by 1-(3-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)hydrazine (382 mg, 1844 μmol) and 4-(dimethylamino)pyridine (18.8 mg, 154 μmol); both added as solids. The heterogeneous solution was stirred at 0° C. for 1 h, then allowed to warm to rt and stir for 18 h. The mixture was quenched with saturated aqueous NaHCO3 (50 mL) and the resulting mixture was extracted with CH2Cl2 (3×50 mL). The combined organic layers were concentrated (heating to 50° C.) and the residue purified by SiO2 chromatography solvent system: CH2Cl2:MeOH 99%:1% gradient 90:10 CH2Cl2 to yield 2,2-difluoro-N′-(3-fluoro-5-(1-methyl-1H-pyrazol-4-yl)pyridin-2-yl)-2-(3-methoxyquinolin-6-yl)acetohydrazide (225 mg, 33.1% yield) as a brown amorphous solid.

المصدر