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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 222071Generated: October 30, 2026

tert-Butoxy bis(dimethylamino)methane → HCID 57747322, compound

https://huagongshe.com/reaction/222071

Reaction equation

Participants

RoleNameHCIDCharge
Reactanttert-Butoxy bis(dimethylamino)methaneHCID 79885—
ReactantHCID 68805818HCID 68805818—
SolventDimethylformamideHCID 6228—
ProductHCID 57747322HCID 5774732267%

Reaction Conditions

Temperature60 °C

Reaction Steps

A dried flask under argon was charged with methyl 4-(4-(4-bromo-2,6-dimethylphenylamino)-6-methyl-5-nitropyrimidin-2-ylamino)benzonitrile (4.3 g, 9.5 mmol) dissolved in anhydrous DMF (95 ml) followed by tert-butoxybis(dimethylamino)methane (2.4 ml, 11.4 mmol). The reaction mixture was heated to 60° C. and stirred overnight under argon. Upon completion the reaction was cooled to ambient temperature, concentrated to half volume, and quenched with H2O (100 ml). The aqueous solution was extracted with ethyl acetate (3×70 ml) and the collected organic fractions were washed with brine (100 ml), dried with MgSO4, filtered and concentrated. Silica gel chromatography (ethyl acetate: Hexanes=50:50) yielded (E)-4-(4-(4-bromo-2,6-dimethylphenylamino)-6-(2-(dimethylamino)vinyl)-5-nitropyrimidin-2-ylamino)benzonitrile (3.21 g, 67%) as a brown solid. m/z=508 [M+1].

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08207178B2
Source datasetuspto-grants-2012_06
ORD IDord-4a73ec64bd97499fbc774bef395555f4
Source noteuspto-grants-2012_06