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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1106181생성일: 2026년 10월 27일

Chlorotrimethylsilane → 6-[4-(N-acetyl-L-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid

https://huagongshe.com/reaction/1106181

반응식

참여 물질

역할이름HCID투입량
반응물ChlorotrimethylsilaneHCID 6397—
반응물4-MethylmorpholineHCID 7972—
반응물Isobutyl chloroformateHCID 62365—
반응물N-Acetyl-L-prolineHCID 66141—
반응물6-(4-Aminophenyl)-1,2-dihydro-2-oxonicotinic acidHCID 12918956—
용매IsopropanolHCID 3776—
용매DichloromethaneHCID 6344—
용매TriethylamineHCID 8471—
생성물6-[4-(N-acetyl-L-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acidHCID 1291896452.2%

반응 단계

To a suspension of 5.75 g (25 m mol) 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid and 175 ml of dichloromethane, 10.2 ml (75 m mol) triethylamine and 9.5 ml (75 m mol) chlorotrimethylsilane are added and the reaction mixture stirred at room temperature for 1 hour. To a solution of 7.86 g (50 m mol) of N-Acetyl-L-proline in 100 ml of dichloromethane at -10° C., 5.5 ml (50 m mol) of N-methylmorpholine and 6.5 ml (50 m mol) of isobutyl chloroformate are added and stirred at -10° C. for 1/2 hour. To this cold mixed anhydride mixture is added the silylated 6-(4-aminophenyl)-1,2-dihydro-2-oxonicotinic acid and the resulting mixture is stirred for 3 hrs in an ice bath and overnight at room temperature. Next, 25 ml of isopropanol is added to the reaction mixture and stirred. The reaction mixture is evaporated and the residue is triturated with ice and water. The solid is collected by filtration and washed with water, isopropanol and ether to yield 4.82 g of 6-[4-(N-Acetyl-L-prolylamino)phenyl]-1,2-dihydro-2-oxonicotinic acid, m.p. 288°-290° dec. From the filtrate an additional 3.94 g of product is obtained.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04311698
출처 데이터셋uspto-grants-1982_01
ORD IDord-a32169fd10f041cba76822b2e56e71c9
출처 메모uspto-grants-1982_01