HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1161664Generated: October 27, 2026
Water → 1-(2-Chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-ol
https://huagongshe.com/reaction/1161664
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Piperidin-4-ol | HCID 79341 | — |
| Reactant | 2,4-Dichloro-6-phenylpyrimidine | HCID 241554 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | 1-(2-Chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-ol | HCID 58626078 | — |
| Product | 1-(4-Chloro-6-phenyl-pyrimidin-2-yl)-piperidin-4-ol | HCID 58626127 | — |
Reaction Steps
A mixture of compound, 2,4-dichloro-6-phenyl-pyrimidine (13 g, 57.77 mmol), piperidin-4-ol (2.9 g, 28.88 mmol) and triethylamine (32.14 mL, 231.11 mmol) in butanol (110 mL) was stirred at 120° C. for 12 hours under nitrogen atmosphere. The reaction mixture was then poured into water (250 mL) and extracted with ethyl acetate (3×50 mL). The organic layers were collected, combined, washed with water (50 mL), dried over anhydrous sodium sulphate, and concentrated under vacuum. The residue thus obtained was purified by column chromatography using ethyl acetate-petroleum ether to give the two compounds, 1-(4-chloro-6-phenyl-pyrimidin-2-yl)-piperidin-4-ol and 1-(2-chloro-6-phenyl-pyrimidin-4-yl)-piperidin-4-ol in ratio 1:4 (overall yield: 51%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07820654B2 |
|---|
| Source dataset | uspto-grants-2010_10 |
|---|
| ORD ID | ord-58b9974ee23e462f936c2eca623109c8 |
|---|
| Source note | uspto-grants-2010_10 |
|---|