Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 477682생성일: 2026년 10월 24일
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/ko/reaction/477682
참여 물질
| 역할 | 이름 | HCID | 투입량 |
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| 반응물 | 2-(Methylthio)thiazolo[5,4-b]pyridine | HCID 699840 | — |
| 반응물 | N-[1-(2-aminoethyl)-4-piperidinyl]-1-(4-fluorophenylmethyl)-1H-benzimidazol-2-amine | HCID 12891741 | — |
| 생성물 | N-[2-[4-[[1-[(4-fluorophenyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinyl]ethyl]thiazolo[5,4-b]pyridin-2-amine | HCID 13983104 | 25% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US04888426 |
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| 출처 데이터셋 | uspto-grants-1989_12 |
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| ORD ID | ord-7b2a4587180f4856a7506462e00fc30d |
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| 출처 메모 | uspto-grants-1989_12 |
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