HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2222245Generated: October 27, 2026
Methylamine → 5-bromo-2-chloro-N-methylpyrimidin-4-amine
https://huagongshe.com/reaction/2222245
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methylamine | HCID 6329 | — |
| Reactant | 5-Bromo-2,4-dichloropyrimidine | HCID 289973 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 5-bromo-2-chloro-N-methylpyrimidin-4-amine | HCID 10727771 | 75% |
Reaction Steps
5-Bromo-2,4-dichloro-pyrimidine (2.41 g, 10.6 mmol) is slowly treated with methylamine (8 M in EtOH, 3.3 mL) in THF (15 mL) at about −20° C. After stirring for 30 minutes at about −20° C., the reaction mixture is partitioned between CHCl3 and saturated NaHCO3. The aqueous layer is extracted with additional CHCl3 twice and the combined organic layer is dried over MgSO4, filtered and concentrated. The crude product is purified by column chromatography (SiO2, EtOAc/Hexane=3/7) to give 1.76 g (75%) of (5-bromo-2-chloro-pyrimidin-4-yl)-methylamine as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07371750B2 |
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| Source dataset | uspto-grants-2008_05 |
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| ORD ID | ord-a435d97d10b74d0d93978be0ac94c0f1 |
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| Source note | uspto-grants-2008_05 |
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