HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219703Generated: October 27, 2026
Triethylamine → Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl ester
https://huagongshe.com/reaction/219703
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Propanol, 3-chloro-, acetate | HCID 12334 | — |
| Reactant | 2-tert-Butyl-4-cyclobutyl-6-(piperazin-1-yl)pyrimidine | HCID 66673390 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Acetic acid 3-[4-(2-tert-butyl-6-cyclobutyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl ester | HCID 69025431 | — |
Reaction Steps
5.5 g of 2-tert-butyl-4-piperazin-1-yl-6-cyclobutyl-pyrimidine (20.0 mmol), 3.15 g of acetic acid 3-chloro-propyl ester (23.1 mmol) and 2.76 g of triethylamine (27.3 mmol) were dissolved in 70 ml of dimethylformamide and stirred for 12 h at 80° C. After cooling, the dimethylformamide was evaporated, and the reaction mixture was partitioned between water and ethyl acetate. The organic layer was dried over magnesium sulfate, filtered, and the solvent was evaporated. The crude product (7 g) was directly used in the subsequent reaction step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08202868B2 |
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| Source dataset | uspto-grants-2012_06 |
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| ORD ID | ord-9f63be50d3af44f18c736260120ee1a6 |
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| Source note | uspto-grants-2012_06 |
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