HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1696730Generated: October 31, 2026
Methylamine → 1-(6-Amino-4-bromo-pyridin-2-yl)-3-methyl-urea
https://huagongshe.com/reaction/1696730
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | 4-Bromo-2,6-diaminopyridine | HCID 11435393 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-(6-Amino-4-bromo-pyridin-2-yl)-3-methyl-urea | HCID 67273920 | — |
Reaction Steps
To a solution of 0.188 g 2.6-diamino-4-bromopyridine in 2 ml acetonitrile was added 0.164 g 1,1-carbonyldi(1,2,4-triazole) and the mixture was stirred at room temperature. After a short period of a clear solution a suspension formed. The mixture was stirred at room temperature for 1 h. To the resulting suspension was added 0.5 ml of a methylamine solution in THF (ca 3 M) and the resulting solution was stirred at room temperature for 0.5 h. The mixture was partitioned between water and ethyl acetate. The phases were separated and the organic phase evaporated to dryness. The residue was taken up in methanol whereby crystallisation occurred. The crystals were collected by filtration and dried to constant weight to yield 0.196 g of the title compound as white crystals. MS (ISP) M+H+243.3; 245.2
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08163778B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-3eda86f27f594dbaab1caf8e3c02fbe6 |
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| Source note | uspto-grants-2012_04 |
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