HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1369961Generated: October 25, 2026
Ethyl Acetate → Methyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate
https://huagongshe.com/reaction/1369961
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Cyanamide | HCID 9864 | — |
| Reactant | HCID 178500902 | HCID 178500902 | — |
| Solvent | Water | HCID 962 | — |
| Product | Methyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate | HCID 10424248 | 8.4% |
Reaction Steps
A suspension of 1.33 g of methyl 2-[1-amino-1-(4-fluorophenyl)methylene]-4-methyl-3-oxopentanoate (5.00 mmol) in 4.20 g of 50% strength aqueous cyanamide solution (50.0 mmol) was heated to reflux. After 17 h, it was cooled to room temperature and treated with ethyl acetate (5 ml) and water (5 ml). The undissolved solid was filtered off. The organic phase was separated off and the aqueous phase was extracted with ethyl acetate (2×5 ml). The combined organic phases were dried over magnesium sulphate and concentrated in vacuo. The crude product (0.97 g) was purified by flash chromatography on silica gel (eluent: methylene chloride). 121.6 mg of methyl 2-amino-4-(4-fluorophenyl)-6-isopropylpyrimidine-5-carboxylate were obtained in the form of a colourless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06579984B1 |
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| Source dataset | uspto-grants-2003_06 |
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| ORD ID | ord-7a93166462b64cdebc1e56a9a6383143 |
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| Source note | uspto-grants-2003_06 |
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