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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 442217생성일: 2026년 10월 26일

2-Cyano-3-[5-(methylsulfanyl)-2-nitrophenyl]prop-2-enamide → 6-Methylthio-2-Aminoquinoline-3-Carboxamide

https://huagongshe.com/reaction/442217

반응식

참여 물질

역할이름HCID투입량
반응물2-Cyano-3-[5-(methylsulfanyl)-2-nitrophenyl]prop-2-enamideHCID 53919854—
촉매IronHCID 23925—
용매acetic acid N,N-dimethylformamideHCID 21926011—
생성물6-Methylthio-2-Aminoquinoline-3-CarboxamideHCID 22752820—

반응 조건

온도75 °C

반응 단계

A mixture of α-cyano-β-(2-nitro-5-methylthiophenyl)acrylamide (8,4 g., 0.032 mole) in acetic acid - N,N-dimethylformamide (110 ml. of 1:1) is heated in a 75° C. bath. Iron powder (2.0g.) is added and the mixture stirred until the internal temperature rose to 95° C. Additional iron powder (6.16 g. total iron added=0.146 mole) is added in small portions over a 15 minute period. The reaction mixture is stirred for one hour following completion of addition and then filtered hot. The iron residue is washed with hot acetic acid and the combined filtrate and wash solution poured into IN hydrochloric acid (200 ml.) The hydrochloride salt which separates is filtered off and dissolved in hot dilute aqueous sodium hydroxide. The yellow solid which separates on cooling is filtered off, washed with isopropyl alcohol and air-dried. Yield = 3.26 g. (44%), M.P. 229°-242° C.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04044134
출처 데이터셋uspto-grants-1977_08
ORD IDord-7eab86348a40463eaba17a480c9f4c05
출처 메모uspto-grants-1977_08