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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2171485Generated: November 1, 2026

Water → N6-{2-[(7-Chloroimidazo[1,2-c]pyrimidin-5-yl)amino]ethyl}-3-nitropyridine-2,6-diamine

https://huagongshe.com/reaction/2171485

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantDiisopropylethylamineHCID 81531—
Reactant5,7-Dichloroimidazo[1,2-c]pyrimidineHCID 46942117—
ReactantN6-(2-aminoethyl)-3-nitropyridine-2,6-diamine trifluoroacetateHCID 86641361—
SolventDimethyl SulfoxideHCID 679—
ProductN6-{2-[(7-Chloroimidazo[1,2-c]pyrimidin-5-yl)amino]ethyl}-3-nitropyridine-2,6-diamineHCID 59312884—

Reaction Conditions

Temperature120 °C

Reaction Steps

800 mg (4.13 mmol) of 5,7-dichloroimidazo[1,2-c]pyrimidine (Example 11A) are suspended in 20 ml of DMSO, and 1.62 g (4.54 mmol) of N6-(2-aminoethyl)-3-nitropyridine-2,6-diamine trifluoroacetate (Example 15A) and 1.6 g (12.38 mmol) of DIPEA are added. The mixture is heated at 120° C. for 16 h. After this time, water is added, and the precipitate which has separated out is filtered off with suction. It is washed with a little 2-propanol/water and the resulting solid is dried under high vacuum. 1.34 g (92% of theory) of the product are obtained as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051323B2
Source datasetuspto-grants-2015_06
ORD IDord-b1ad431128e64ac28c69167a5215e102
Source noteuspto-grants-2015_06