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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403178Generated: October 31, 2026

Dimethylformamide → N'-(5-fluoro-2-methylsulfanylpyrimidin-4-yl)-N,N-dimethylformamidine

https://huagongshe.com/reaction/1403178

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant5-Fluoro-2-(methylthio)pyrimidin-4-amineHCID 20593351—
SolventDiethyl EtherHCID 3283—
ProductN'-(5-fluoro-2-methylsulfanylpyrimidin-4-yl)-N,N-dimethylformamidineHCID 5831893284%

Reaction Steps

To a solution of 5-fluoro-2-methylsulfanylpyrimidin-4-ylamine (7.5 g, 47.1 mmol) in N,N-dimethylformamide (DMF; 18 mL) was added DMF-dimethylacetal (DMF-DMA; 8.42 g, 70.7 mmol), and the resulting solution was stirred under nitrogen (N2) for 4 h. The homogeneous solution was diluted with diethyl ether (Et2O; 500 mL), washed with H2O (5×100 mL), and the organic phase was dried over Na2SO4, filtered, and concentrated to a white solid. Recrystallization from hexane afforded N′-(5-fluoro-2-methylsulfanylpyrimidin-4-yl)-N,N-dimethylformamidine (8.47 g, 84%) as white needles: mp 75-77° C.; 1H NMR (400 MHz, CDCl3) δ 8.67 (s, 1H), 8.12 (d, J=3.1 Hz, 1H), 3.19 (s, 3H), 3.18 (s, 3H), 2.53 (s, 3H); CIMS m/z 214 ([M]+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912207B2
Source datasetuspto-grants-2014_12
ORD IDord-0cb777d5fc4b401ba7efa6841c03dfec
Source noteuspto-grants-2014_12