Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Fluoroaniline | HCID 9731 | — |
| Reactant | Ethyl 4-chloro-2-methylthio-pyrimidine-5-carboxylate | HCID 53249641 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 86585952 | HCID 86585952 | 76.6% |
Reaction Steps
To a solution of ethyl 4-chloro-2-methylthiopyrimidine-5-carboxylate (Aldrich, 24 g, 103 mmol) in 250 mL of acetonitrile at room temperature was added 4-fluoroaniline (22.75 g, 205 mmol). After stirring for two days, the mixture was heated at 60° C. for four hours. The resulting solid was filtered and washed with EtOAc. The filtrate was concentrated, diluted in EtOAc (300 L), washed with brine, dried (MgSO4), filtered and concentrated to provide a crude product. The crude product was stirred with hexanes (400 mL) and then filtered to give 23 g of the ethyl 4-(4-fluorophenyl)amino-2-methylthiopyrimidine-5-carboxylate as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06506749B2 |
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| Source dataset | uspto-grants-2003_01 |
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| ORD ID | ord-09b88aac48634f05a38a88d3e0d1226f |
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| Source note | uspto-grants-2003_01 |
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