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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516834Generated: November 4, 2026

N'-(1-benzyl-4-methyl-5-nitro-6-oxopyrimidin-2-yl)-N,N-dimethylmethanimidamide → N'-[1-benzyl-4-[(E)-2-(dimethylamino)ethenyl]-5-nitro-6-oxopyrimidin-2-yl]-N,N-dimethylmethanimidamide

https://huagongshe.com/reaction/1516834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN'-(1-benzyl-4-methyl-5-nitro-6-oxopyrimidin-2-yl)-N,N-dimethylmethanimidamideHCID 11186127—
SolventDimethylformamideHCID 6228—
ProductN'-[1-benzyl-4-[(E)-2-(dimethylamino)ethenyl]-5-nitro-6-oxopyrimidin-2-yl]-N,N-dimethylmethanimidamideHCID 15376104—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of (E)-N′(1-benzyl-4-methyl-5-nitro-6-oxo-1,6-dihydropyrimidin-2-yl)-N,N-dimethylformimidamide (64.7 g, 0.2 mol) in DMF (254 mL) was added DMF-dimethylacetal (54.5 mL, 0.41 mol). The reaction mixture was stirred for 3 h at 65° C., cooled, and the solvent was removed under reduced pressure. The residue was triturated with ethanol, and the solid was collected by vacuum filtration (69.2 g, 91%) and used in the next step without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08227601B2
Source datasetuspto-grants-2012_07
ORD IDord-fbf38190112b4f2c9343b38e4a117a90
Source noteuspto-grants-2012_07