Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Bromoform | HCID 5558 | — |
| Reactant | 2-Methylpentane | HCID 7892 | — |
| Reactant | Isoamyl Nitrite | HCID 8053 | — |
| Reactant | 5-Bromo-4-methylpyrimidin-2-amine | HCID 18616196 | — |
| Product | 2,5-Dibromo-4-methylpyrimidine | HCID 66521322 | — |
Reaction Steps
Isoamylnitrite (21 ml) was added to a stirred suspension of 5-bromo-4-methyl-2-pyrimidinamine (1.75 g) in bromoform (30 ml) and the mixture heated at 85° C. for 4 h. After cooling, isohexane (300 ml) was added and the solution passed through a pad of silica-gel. The silica was washed with petrol (1000 ml), dichloromethane (200 ml) then the product eluted with ethylacetate. The ethylacetate layer was evaporated under reduced pressure and the residue purified by chromatography on silica eluting with 5% diethylether/isohexane, yield 0.9 g
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08158820B2 |
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| Source dataset | uspto-grants-2012_04 |
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| ORD ID | ord-60cbfb6a2e3b4955bf8c0e02034929f5 |
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| Source note | uspto-grants-2012_04 |
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