HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2053090Generated: October 30, 2026
Ethyl Acetate → 2-Methylsulfanyl-6-(3-trifluoromethylphenyl)-pyrimidin-4-ylamine
https://huagongshe.com/reaction/2053090
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Amino-6-chloro-2-methylthiopyrimidine | HCID 70496 | — |
| Reactant | 3-(Trifluoromethyl)phenylboronic acid | HCID 2734388 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 2-Methylsulfanyl-6-(3-trifluoromethylphenyl)-pyrimidin-4-ylamine | HCID 58513228 | 60.7% |
Reaction Steps
To a stirred solution of 4-amino-6-chloro-2-methylthiopyrimidine (3.5 g) in toluene (45 mL) under a nitrogen atmosphere was added, sequentially, (3-trifluoromethylphenyl)boronic acid (4.15 g), potassium carbonate (25 mL, 2M) and tetrakis(triphenylphosphine)palladium(0) (1.16 g). The mixture was heated to reflux for ten hours and stirred at room temperature over the weekend. Ethyl acetate (150 mL) was added and the mixture washed with water (2×100 mL). Organics were separated, washed with saturated sodium chloride (100 mL), dried over sodium sulphate and solvent was evaporated under reduced pressure to yield crude product. Purification by flash chromatography yielded product 2-methylsulfanyl-6-(3-trifluoromethyl-phenyl)-pyrimidin-4-ylamine (3.45 g)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07326715B2 |
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| Source dataset | uspto-grants-2008_02 |
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| ORD ID | ord-0826825d8ea24d95b250cc29bdfd2742 |
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| Source note | uspto-grants-2008_02 |
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