HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 574263Generated: October 29, 2026
Potassium Carbonate → {(R)-2-[3-(2,6-difluoro-benzyl)-2,6-dioxo-5-(2-oxo-pyrrolidin-1-yl)-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester
https://huagongshe.com/reaction/574263
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | {(R)-2-[5-(4-chloro-butyrylamino)-3-(2,6-difluoro-benzyl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester | HCID 67144080 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | {(R)-2-[3-(2,6-difluoro-benzyl)-2,6-dioxo-5-(2-oxo-pyrrolidin-1-yl)-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester | HCID 67143540 | 90% |
Reaction Steps
{(R)-2-[5-(4-chloro-butyrylamino)-3-(2,6-difluoro-benzyl)-2,6-dioxo-3,6-dihydro-2H-pyrimidin-1-yl]-1-phenyl-ethyl}-carbamic acid tert-butyl ester (30 mg, 0.052 mmol) and potassium carbonate (30 mg, 0.217 mmol) were dissolved at room temperature for 6 hrs in DMF (1 mL) with stirring. The solution was diluted with dichloromethane and washed with water to separate an organic layer. After concentration of the organic layer, the residue was purified using silica gel chromatography (eluent: dichloromethane/methanol, 30/1) and dried in a vacuum to afford 25 mg of the compound as a colorless oil (yield 90%). 1H NMR (300 MHz, CDCl3) δ 1.34 (9H, s), 2.15 (2H, p), 2.51 (2H, t), 3.80 (2H, m), 4.03 (1H, m), 4.27 (1H, m), 4.98-5.13 (3H, m), 5.57 (1H, d), 6.97 (2H, m), 7.22-7.40 (6H, m), 7.62 (1H, s)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09034850B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-8ee10643686c4683a4322a22fae5a7ef |
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| Source note | uspto-grants-2015_05 |
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