돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 604577생성일: 2026년 10월 25일

Pyridine → N-[4-acetyl-5-(2-methanesulfonylaminoethyl)-5-phenyl-4,5-dihydro-1,3,4-thiadiazol-2-yl]-2-phenylpropanamide

https://huagongshe.com/reaction/604577

반응식

참여 물질

역할이름HCID투입량
반응물PyridineHCID 1049—
반응물2-Phenylpropionic acid, (-)-HCID 446626—
반응물(R)-2-phenylpropionyl chlorideHCID 7161075—
반응물HCID 67039184HCID 67039184—
용매Thionyl ChlorideHCID 24386—
생성물N-[4-acetyl-5-(2-methanesulfonylaminoethyl)-5-phenyl-4,5-dihydro-1,3,4-thiadiazol-2-yl]-2-phenylpropanamideHCID 6703918012%

반응 단계

Next, (R)-(−)-2-phenylpropionyl chloride prepared from (R)-(−)-2-phenylpropionic acid (4.65 g, 3.10 mmol) and thionyl chloride (30 mL), and N-[2-(3-acetyl-5-amino-2-phenyl-2,3-dihydro-1,3,4-thiadiazol-2-yl)ethyl]methane-sulfonamide obtained above were treated in pyridine (5.0 mL, 61.8 mmol) in the same manner as that in Step 1 of Example 20, and the resultant was purified by silica gel column chromatography (chloroform/n-hexane/ethyl acetate/methanol=20/3/2/1) to give one diastereomer of N-[4-acetyl-5-(2-methanesulfonylaminoethyl)-5-phenyl-4,5-dihydro-1,3,4-thiadiazol-2-yl]-2-phenylpropanamide (0.75 g, 12%) as a fraction eluted first, and another diastereomer of N-[4-acetyl-5-(2-methane-sulfonylaminoethyl)-5-phenyl-4,5-dihydro-1,3,4-thiadiazol-2-yl]-2-phenylpropanamide (0.82 g, 13%) as a fraction eluted later.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07910611B2
출처 데이터셋uspto-grants-2011_03
ORD IDord-095cd61b2e274ae98ade817cc9ffd5c0
출처 메모uspto-grants-2011_03