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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1681727Generated: November 4, 2026

Pyridine → HCID 10349022, compound

https://huagongshe.com/reaction/1681727

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantAcetic AnhydrideHCID 7918—
ReactantHCID 10031247HCID 10031247—
SolventDichloromethaneHCID 6344—
ProductHCID 10349022HCID 10349022—

Reaction Steps

To a solution of 2-chloro-8,9-dihydro-7-[(hydroxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]-10-methylpyrido[1,2-a]indol-6(7H)-one (1.64 g) in dichloromethane (32 ml) were added pyridine (0.83 ml) and acetic anhydride (0.53 ml). The solution was refluxed for 24 hours. After being cooled, the solution was washed with water twice and brine, dried over sodium sulfate, and evaporated, to give 7-[(acetoxy)(5-methyl-1-trityl-1H-imidazol-4-yl)methyl]-2-chloro-8,9-dihydro-10-methylpyrido[1,2-a]indol-6(7H)-one (1.49 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05173493
Source datasetuspto-grants-1992_12
ORD IDord-70b6aabb183d4177a1b2045a7de7167c
Source noteuspto-grants-1992_12