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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5,7-Dichloroimidazo[1,2-c]pyrimidine | HCID 46942117 | — |
| Reactant | N6-(2-aminoethyl)-3-nitropyridine-2,6-diamine trifluoroacetate | HCID 86641361 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | N6-{2-[(7-Chloroimidazo[1,2-c]pyrimidin-5-yl)amino]ethyl}-3-nitropyridine-2,6-diamine | HCID 59312884 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09051323B2 |
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| Source dataset | uspto-grants-2015_06 |
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| ORD ID | ord-b1ad431128e64ac28c69167a5215e102 |
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| Source note | uspto-grants-2015_06 |
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