HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 56221Generated: October 25, 2026
Acetamide → 3-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-2,6-dimethyl-pyrimidin-4(3H)-one
https://huagongshe.com/reaction/56221
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetamide | HCID 178 | — |
| Reactant | O-Xylene | HCID 7237 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | N-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-3-oxobutan-amide | HCID 90022774 | — |
| Catalyst | Titanium isopropoxide | HCID 11026 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 3-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-2,6-dimethyl-pyrimidin-4(3H)-one | HCID 90022936 | 29.7% |
Reaction Steps
A mixture of N-(3-fluoro-4-((3-(tetrahydrofuran-2-yl)propyl)amino)phenyl)-3-oxobutanamide (250 mg, 0.78 mmol), acetamide (92 mg, 1.56 mmol), titanium tetraisopropanolate (1.9 mL) and xylene (10 mL) was stirred at 165° C. for 24 h. The mixture was then cooled to rt. 60 mL of toluene and 60 mL of saturated NH4Cl aqueous solution were added and the resulting mixture was stirred further at rt overnight. The mixture was then filtered and the filtrate was extracted with DCM (15 mL×3). The combined organic layers were washed with brine (15 mL×2), dried over anhydrous Na2SO4 and concentrated in vacuo. The residue was purified by a silica gel column chromatography (PE/EtOAc (V/V)=1:2) to give the title compound as a yellow solid (80 mg, 29%). The compound was characterized by the following spectroscopic data:
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09434695B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-3dbf39e8ebda4244a9c3ea891f60787c |
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| Source note | uspto-grants-2016_09 |
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