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HRID 521131Erstellt: 26. Oktober 2026

1-Methyl-1H-benzimidazole-5-carboxylic acid → (cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-(1-methyl-1H-benzoimidazol-5-yl)-methanone

https://huagongshe.com/reaction/521131

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Methyl-1H-benzimidazole-5-carboxylic acidHCID 4913063—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Eduktcis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridineHCID 58123900—
Produkt(cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-(1-methyl-1H-benzoimidazol-5-yl)-methanoneHCID 6722421490%

Reaktionsschritte

The title compound is prepared from 1-methyl-1H-benzoimidazole-5-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: 90% of theory; LC (method 4): tR=1.62 min; Mass spectrum (ESI+): m/z=332 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09328072B2
Quelldatensatzuspto-grants-2016_05
ORD IDord-aff95a58d8524529baac9e0c3f77248d
Quellennotizuspto-grants-2016_05