HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 219711Generated: October 30, 2026
Sodium Iodide → Acetic acid 3-[4-(2-tert-butyl-6-cyclopropyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl ester
https://huagongshe.com/reaction/219711
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Propanol, 3-chloro-, acetate | HCID 12334 | — |
| Reactant | 2-Tert-butyl-4-piperazin-1-yl-6-cyclopropyl-pyrimidine | HCID 67372611 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Acetic acid 3-[4-(2-tert-butyl-6-cyclopropyl-pyrimidin-4-yl)-piperazin-1-yl]-propyl ester | HCID 69026905 | — |
Reaction Steps
2.9 g of 2-tert-Butyl-4-piperazin-1-yl-6-cyclopropyl-pyrimidine (11.1 mmol), 1.8 g acetic acid 3-chloro-propyl ester (13.2 mmol), 1.38 g of triethylamine (13.7 mmol), and a spatula tip of sodium iodide were dissolved in 50 ml of dimethylformamide and stirred for 8 h at 80° C. After cooling to room temperature, the dimethylformamide was evaporated. 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 (3.7 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-184b0733e8444260864a6e980e6ad5c3 |
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| Source note | uspto-grants-2012_06 |
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