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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2199219생성일: 2026년 10월 26일

Cyanamide → 3-[cyano(methyl)sulfonimidoyl]-N-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-2-methylpropanamide

https://huagongshe.com/reaction/2199219

반응식

참여 물질

역할이름HCID투입량
반응물CyanamideHCID 9864—
반응물2-[2-(Carboxylatomethyl)-3-iodophenyl]acetateHCID 21945688—
반응물N-[2-(5-fluoro-pyridin-3-yl)-4-methyl-thiazol-5-yl]-2-methyl-3-methylsulfanyl-propionamideHCID 59580474—
용매DichloromethaneHCID 6344—
생성물3-[cyano(methyl)sulfonimidoyl]-N-[2-(5-fluoropyridin-3-yl)-4-methyl-1,3-thiazol-5-yl]-2-methylpropanamideHCID 5958058675.9%

반응 단계

To a solution of N-[2-(5-fluoro-pyridin-3-yl)-4-methyl-thiazol-5-yl]-2-methyl-3-methylsulfanyl-propionamide (0.250 g, 0.76 mmol) in dichloromethane (3.07 ml) at 0° C. was added cyanamide (0.064 g, 1.53 mmol) and iodobenzenediacetate (0.272 g, 0.84 mmol) and subsequently stirred at room temperature for 1 hour. The reaction was concentrated to dryness. The crude material was purified by silica gel column chromatography (10% methanol/ethyl acetate) to give the desired product as a light yellow solid (0.220 g, 60%): mp 75-81° C.; 1H NMR (400 MHz, CDCl3) δ 9.85 (s, 1H), 8.94-8.70 (m, 1H), 8.57-8.34 (m, 1H), 8.07-7.77 (m, 1H), 3.69-3.40 (m, 2H), 3.22-3.00 (m, 1H), 2.92-2.77 (m, 3H), 2.50 (m, 3H), 1.49 (m, 3H); ESIMS m/z 363.9 (M−2).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09357780B2
출처 데이터셋uspto-grants-2016_06
ORD IDord-6b92aa137377485898fa9b62dc4778a9
출처 메모uspto-grants-2016_06