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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477682생성일: 2026년 10월 25일

2-(Methylthio)thiazolo[5,4-b]pyridine → N-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]thiazolo[5,4-b]pyridin-2-amine

https://huagongshe.com/reaction/477682

반응식

참여 물질

역할이름HCID투입량
반응물2-(Methylthio)thiazolo[5,4-b]pyridineHCID 699840—
반응물N-[1-(2-aminoethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amineHCID 12891741—
생성물N-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]thiazolo[5,4-b]pyridin-2-amineHCID 1398310425%

반응 조건

온도140 °C

반응 단계

A mixture of 2.8 parts of 2-(methylthio)thiazolo[5,4-b]pyridine and 5.5 parts of N-[1-(2-aminoethyl)-4-piperidinyl]-1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-amine was stirred for 24 hours at 140° C. The reaction mixture was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol, saturated with ammonia, (97:3 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized from acetonitrile. The product was filtered off and dried, yielding 1.9 parts (25%) of N-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]thiazolo[5,4-b]pyridin-2-amine; mp. 203.5° C. (compound 103).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04888426
출처 데이터셋uspto-grants-1989_12
ORD IDord-7b2a4587180f4856a7506462e00fc30d
출처 메모uspto-grants-1989_12