Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Ammonium Hydroxide | HCID 14923 | — |
| Reactant | HCID 18799649 | HCID 18799649 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 492831 | HCID 492831 | 94% |
Reaction Steps
A flask is charged with 4,6-dichloro-2-(1-(2-pyridyl)ethyl)thio-pyrimidine (0.560 g, 1.96 mmol), acetonitrile (6.5 ml) and 13 ml of 29 % NH4OH. The contents are stirred at 35° C. for 15 h, poured into 50 ml of water, extracted once with ethyl acetate. The organic layer is washed with a saturated solution of brine (1×30 ml), dried with anhydrous Na2SO4 and concentrated in vacuo. Chromatography is accomplished with 100 g of silica gel, packed and eluted with ethyl acetate-hexane (2:3), to yield 0.491 g (94%) of 4-amino-6-chloro-2-(1-(2-pyridyl)ethyl)thio-pyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06043248 |
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| Source dataset | uspto-grants-2000_03 |
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| ORD ID | ord-d3e0aadb222840fb802d94df5cf5f6c1 |
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| Source note | uspto-grants-2000_03 |
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