Triethylamine → 4-amino-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl)benzamide

In a 100 mL three-necked round-bottomed flask fitted with a mechanical stirrer, nitrogen inlet and thermometer was placed 0.62 g (3 mmol) of 4-amino-3,5-dichlorobenzoic acid, 20 mL of tetrahydrofuran, and 1.52 g (15 mmol) of triethylamine. To the resulting well-stirred mixture was added 0.4 g (3.3 mmol) of methanesulfonyl chloride dropwise while keeping the reaction temperature at -25° C. The resulting suspension was stirred at -25° C. for 30 minutes, after which 0.7 g (3.8 mmol) of 3-amino-1-chloro-3-methyl-2-pentanone hydrochloride was added slowly over a 45 minute period. After the addition was complete, the reaction mixture was stirred at -25° C. for an additional 60 minutes. The cooling bath was removed; the reaction mixture was allowed to warm to room temperature and stirred for 3 hours. The reaction mixture was poured into a mixture of water and ethyl acetate. The phases were separated and the aqueous layer was extracted several times with ethyl acetate. The combined organic phases were washed sequentially with water, saturated aqueous sodium bicarbonate, and water, then dried over anhydrous magnesium sulfate. The resulting solution was treated with charcoal and filtered through Celite™. The solvent was removed using a rotary evaporator, yielding 0.84 g of 4-amino-3,5-dichloro-N-(3-chloro-1-ethyl-1-methyl-2-oxopropyl) benzamide as a white solid, mp 134°-138° C.

1. customIn a 100 mL three-necked round-bottomed flask fitted with a mechanical stirrer, nitrogen inlet
2. customat -25° C
3. stirringThe resulting suspension was stirred at -25° C. for 30 minutes
4. additionAfter the addition
5. stirringthe reaction mixture was stirred at -25° C. for an additional 60 minutes
6. customThe cooling bath was removed
7. stirringstirred for 3 hours
8. additionThe reaction mixture was poured into a mixture of water and ethyl acetate
9. customThe phases were separated
10. extractionthe aqueous layer was extracted several times with ethyl acetate
11. washThe combined organic phases were washed sequentially with water, saturated aqueous sodium bicarbonate, and water
12. dry with materialdried over anhydrous magnesium sulfate
13. additionThe resulting solution was treated with charcoal
14. filtrationfiltered through Celite™
15. customThe solvent was removed
16. customa rotary evaporator

ORD 기록

ord-46fe2d65181f4793ba06ed02723bd06a

출처 데이터셋

uspto-grants-1999_02

DOI

10.6084/m9.figshare.5104873.v1

특허 번호

US05874466