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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1665129Generated: October 30, 2026

Dimethylformamide → HCID 178508756, compound

https://huagongshe.com/reaction/1665129

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantTrimethylsilyl iodideHCID 85247—
ReactantHCID 178451396HCID 178451396—
SolventDichloromethaneHCID 6344—
ProductHCID 178508756HCID 178508756—

Reaction Steps

Iodotrimethylsilane (0.23 ml, 1.66 mmol) is added to a suspension of (E)-tert-Butyl 2′-(3,5-diamino-6-chloropyrazine-2-carbonylimino)-8-azaspiro[bicyclo[3.2.1]octane-3,4′-imidazolidine]-8-carboxylate (Ex. 251) (500 mg, 1.11 mmol) in DCM (10 ml). DMF (5 ml) is then added and the reaction is stirred at room temperature overnight. Iodotrimethylsilane (0.5 ml) is added and the reaction mixture is concentrated in vacuo. The yellow solid is suspended in DCM and collected by filtration. The solid is dissolved in 1:1 MeOH/DCM and loaded onto an SCX-2 cartridge eluted with DCM followed by MeOH and NH3/MeOH. The methanolic ammonia fractions are concentrated in vacuo to afford (E)-3,5-diamino-6-chloro-N-(8-azaspiro[bicyclo[3.2.1]octane-3,4′-imidazolidine]-2′-ylidene)pyrazine-2-carboxamide as a yellow gum; [M+H]+ 351

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08039472B2
Source datasetuspto-grants-2011_10
ORD IDord-79ed563614fb4ca0a4aaed0a23263a3d
Source noteuspto-grants-2011_10