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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2114827Generated: November 3, 2026

Tetrahydrofuran → HCID 86612116, compound

https://huagongshe.com/reaction/2114827

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTetrahydrofuranHCID 8028—
Reactant4-(Bromomethyl)pyridineHCID 642799—
ReactantLithium HexamethyldisilazideHCID 2733832—
ReactantHCID 86612117HCID 86612117—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
ProductHCID 86612116HCID 86612116—

Reaction Steps

To a cold (0° C.) solution of 8-(4-fluorobenzyl)-10-toluenesulfonyloxy-3,4,7,8-tetrahydropyrido-[3′,4′:4,5]pyrrolo[1,2-a]pyrazine-1,9(2H,6H)-dione (60 mg, 0.12 mmol) in anhydrous DMF (1 mL), a solution of lithium bis(trimethylsilyl)amide in THF (1 M, 1.5 eq) was added. The mixture was stirred at the same temperature for 30 minutes. A solution of 4-bromomethylpyridine in diethyl ether (generated from the corresponding hydrobromide salt through partition between aq sodium carbonate and ether, and drying the solution by passing it through a plug of activated basic alumina). The reaction mixture was stirred at rt for one hour and concentrated under vacuum. The residue was subjected to reverse phase preparative HPLC purification. Collection and lyophilization of appropriate fractions provided the titled compounds.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07435735B2
Source datasetuspto-grants-2008_10
ORD IDord-5fe0e5660e9e4dca90ed054d9aba34d5
Source noteuspto-grants-2008_10