HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1170739Generated: October 30, 2026
2-Chloro-5-methylpyrimidin-4-amine → HCID 57675111, compound
https://huagongshe.com/reaction/1170739
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloro-5-methylpyrimidin-4-amine | HCID 4302175 | — |
| Reactant | tert-Butyl 4-(4-aminophenoxy)piperidine-1-carboxylate | HCID 22181157 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 57675111 | HCID 57675111 | 95% |
Reaction Steps
A mixture of 2-chloro-5-methylpyrimidin-4-amine (540 mg, 3.7 mmol), tert-butyl 4-(4-aminophenoxy)piperidine-1-carboxylate (1.1 g, 3.7 mmol) was suspended in acetic acid (20 mL) and heated at 70° C. for 1 h. The mixture was allowed to cool to room temperature and acetic acid removed under reduced pressure. The residue was taken in water (20 mL) and neutralized to pH˜7. The resulting solution was extracted with EtOAc (30 mL) and the organic layer separated. The organic layer was washed with brine, dried over MgSO4 and filtered. The filtrate was concentrated in vacuo to afford the title compound (1.4 g, 95%) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07825246B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-f71b6af3735a47c0805bc3829a6fb95c |
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| Source note | uspto-grants-2010_11 |
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