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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 75839생성일: 2026년 10월 24일

Pyridine → (R)-methyl 2-(3-(4-(2-fluorophenylsulfonamido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoate

https://huagongshe.com/ko/reaction/75839

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-Fluorobenzenesulphonyl chlorideHCID 137761—
반응물(R)-methyl 2-(3-(4-aminophenyl)isoxazole-5-carboxamido)-3-methylbutanoateHCID 67352792—
용매DichloromethaneHCID 6344—
생성물(R)-methyl 2-(3-(4-(2-fluorophenylsulfonamido)phenyl)isoxazole-5-carboxamido)-3-methylbutanoateHCID 6735586486%

반응 단계

To a solution of 500 mg (1.57 mmol) of (R)-methyl 2-(3-(4-aminophenyl)isoxazole-5-carboxamido)-3-methylbutanoate (example 151, step 3) in DCM, 1.2 eq of pyridine was added and stirred for 10 minutes, then 368 mg (1.89 mmol) 2-fluorobenzene-1-sulfonyl chloride was added and the reaction mixture was stirred for 3 hours. DCM was removed under vacuum, the reaction mixture was washed with 1NHCl and extracted with EtOAc. The organic layer was concentrated and purified by precipitation using DCM and petroleum ether to yield 410 mg (86%) of title compound. MS (ESI): m/z 476(M+H)+; 1HNMR (DMSO-d6, 300 MHz): δ 11.039 (s, 1H), 9.215 (d, 1H), 7.942 (m, 1H), 7.805 (d, 2H), 7.718 (m, 1H), 7.625 (s, 1H), 7.465 (m, 2H), 7.271(d, 2H), 4.314 (t, 1H), 3.690 (s, 3H), 2.228 (m, 1H), 0.971 (d, 6H).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08835428B2
출처 데이터셋uspto-grants-2014_09
ORD IDord-55309ba916b148068439f137b36f3df1
출처 메모uspto-grants-2014_09