HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 729461Generated: October 30, 2026
Ethyl bromoacetate → Ethyl {5-[2-(4-hydroxypiperidin-1-yl)pyrimidin-5-yl]-2H-tetrazol-2-yl}acetate
https://huagongshe.com/reaction/729461
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[5-(1H-Tetrazol-5-yl)pyrimidin-2-yl]piperidin-4-ol | HCID 178516462 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | Ethyl {5-[2-(4-hydroxypiperidin-1-yl)pyrimidin-5-yl]-2H-tetrazol-2-yl}acetate | HCID 86621801 | — |
Reaction Steps
A mixture of 1-[5-(1H-tetrazol-5-yl)pyrimidin-2-yl]piperidin-4-ol (550 mg, 2.224 mmol), triethylamine (0.62 mL, 4.45 mmol), ethyl bromoacetate (371 μL, 3.34 mmol) in THF (77.4 mL) was heated at 80° C. for 1 h. The solvent was evaporated, diluted with water (5 mL) and slurried with Et2O (5 mL). The mixture was filtered and washed with water followed by Et2O. The solid was dried under high vacuum to afford the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07582633B2 |
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| Source dataset | uspto-grants-2009_09 |
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| ORD ID | ord-0fe8d784f3884c9eac8e72e612daa12b |
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| Source note | uspto-grants-2009_09 |
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