HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2192253Generated: October 29, 2026
Dimethylformamide → 6-(3-bromo-6-(3-nitrophenyl)-1H-indol-1-yl)-N-methylpyrimidin-4-amine
https://huagongshe.com/reaction/2192253
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methylamine hydrochloride | HCID 6364545 | — |
| Reactant | 3-bromo-1-(6-chloropyrimidin-4-yl)-6-(3-nitrophenyl)-1H-indole | HCID 50991544 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(3-bromo-6-(3-nitrophenyl)-1H-indol-1-yl)-N-methylpyrimidin-4-amine | HCID 50991545 | — |
Reaction Steps
DMF (10 mL) was added to a mixture of 3-bromo-1-(6-chloropyrimidin-4-yl)-6-(3-nitrophenyl)-1H-indole (500 mg, 1.16 mmol), methylamine hydrochloride (393 mg, 5.82 mmol) and potassium carbonate (1.60 g, 11.6 mmol). After stirring at 80° C. for 3 hours and then cooling to room temperature, the reaction solution was added to icy water. After stirring at room temperature for 15 hours, thus produced solid was filtered, washed with water and then dried. The target compound (500 mg) was obtained as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08329708B2 |
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| Source dataset | uspto-grants-2012_12 |
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| ORD ID | ord-add1c82e11894a05806007d7545c09b5 |
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| Source note | uspto-grants-2012_12 |
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