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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2360893Generated: October 31, 2026

Imidazo(1,2-a)pyridine-6-carboxylic acid → (cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-imidazo[1,2-a]pyridin-6-yl-methanone

https://huagongshe.com/reaction/2360893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazo(1,2-a)pyridine-6-carboxylic acidHCID 7075376—
ReactantMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Reactantcis-2,3,4,4a,9,9a-hexahydro-1H-indeno[2,1-b]pyridineHCID 58123900—
Product(cis-2,3,4,4a,9,9a-Hexahydro-indeno[2,1-b]pyridin-1-yl)-imidazo[1,2-a]pyridin-6-yl-methanoneHCID 6722343985%

Reaction Steps

The title compound is prepared from imidazo[1,2-a]pyridine-6-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 hexa-fluorophosphate is used]. Yield: 85% of theory; LC (method 3): tR=1.81 min; Mass spectrum (ESI+): m/z=318 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08686149B2
Source datasetuspto-grants-2014_04
ORD IDord-c13076071b854b74be85b9502fca25ff
Source noteuspto-grants-2014_04