HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 450363Generated: October 31, 2026
N-(1-(5-Fluoropyrimidin-2-yl)vinyl)acetamide → HCID 58367416, compound
https://huagongshe.com/reaction/450363
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-(1-(5-Fluoropyrimidin-2-yl)vinyl)acetamide | HCID 45119272 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 58367416 | HCID 58367416 | 95.3% |
Reaction Steps
N-(1-(5-Fluoropyrimidin-2-yl)vinyl)acetamide (Intermediate 12, 0.10 g, 0.55 mmol) in MeOH (5 ml) under N2 was added (+)-1,2-bis((2S,5S)-2,5-diethylphospholano)benzene (cyclooctadiene)rhodium(I)trifluoromethanesulfonate (0.04 g, 0.0055 mmol). The solution was transferred to a high-pressure bomb and charged 150 psi H2. The reaction was stirred at room temperature for 4 hours. The solvent was removed and the resulted residue was purified by column chromatography (EtOAc) to give the title compound as a white solid (0.096 g, 95%). 1H NMR (400 MHz) 8.84 (d, J=0.8 Hz, 2H), 8.34 (d, J=7.6 Hz, 1H), 5.00 (m, 1H), 1.84 (s, 3H), 1.37 (d, J=6.8 Hz, 3H). MS: Calculated: 183. Found: [M+H]+ 184. Enantiomeric excess determined by HPLC (Chiralpak IA; 95:5 CO2/MeOH), >99% ee.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08486966B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-d492bd966a184f91b2113452e16935d9 |
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| Source note | uspto-grants-2013_07 |
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