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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 455486생성일: 2026년 10월 26일

Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1) → (cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-imidazo[1,2-a]pyridin-7-yl-methanone

https://huagongshe.com/reaction/455486

반응식

참여 물질

역할이름HCID투입량
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물Imidazo[1,2-a]pyridine-7-carboxylic acidHCID 18364844—
반응물cis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridineHCID 58123900—
생성물(cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-imidazo[1,2-a]pyridin-7-yl-methanoneHCID 6722318218%

반응 단계

The title compound is prepared from imidazo[1,2-a]pyridine-7-carboxylic acid and cis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridine following a procedure analogous to that described in Example 1 [2-(7-aza-1H-benzotriazol-1-yl)-1,1,3,3-tetramethyluronium hexafluorophosphate is used]. Yield: 18% of theory; LC (method 4): tR=1.56 min; Mass spectrum (ESI+): m/z=318 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08497281B2
출처 데이터셋uspto-grants-2013_07
ORD IDord-593ce40d189d44f3b9cf9e362bcc26c2
출처 메모uspto-grants-2013_07