HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046307Generated: October 26, 2026
Triethylamine → (+/-)-4-Fluoro-2-methoxy-N-[1-(1-methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yl)-ethyl]-benzamide
https://huagongshe.com/reaction/2046307
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diethyl cyanophosphonate | HCID 76257 | — |
| Reactant | 4-Fluoro-2-methoxybenzoic acid | HCID 2774545 | — |
| Reactant | (+/-) 2-(1-amino-ethyl)-1-methyl-1H-[4,4']bipyrimidinyl-6-one | HCID 68527245 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (+/-)-4-Fluoro-2-methoxy-N-[1-(1-methyl-6-oxo-1,6-dihydro-[4,4']bipyrimidinyl-2-yl)-ethyl]-benzamide | HCID 25116210 | 66% |
Reaction Steps
To a solution of 0.112 g (0.48 mmol) of (+/−) 2-(1-amino-ethyl)-1-methyl-1H-[4,4′]bipyrimidinyl-6-one in 5 mL of dimethylformamide was added 0.082 g (0.48 mmol) of 4-fluoro-2-methoxy-benzoic acid and 90 μL (0.58 mmol) of diethyl phosphorocyanidate (DEPC). The resulting mixture was cooled at 0° C., 70 μL (0.53 mmol) of triethylamine was added and stirred at room temperature for 1 h. Water was added and the mixture extracted with diethyl acetate. The extracts were washed with a saturated aqueous solution of ammonium chloride, dried and evaporated. The residue was purified on preparative thin layer chromatography eluting with a mixture of dichloromethane/methanol/aqueous ammonia solution (29%) in the proportions 95/5/0.5 to afford 0.12 g (66%) of the desired compound as a white powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08592436B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-18823f9eb1c84a8097cbd5a40db20c23 |
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| Source note | uspto-grants-2013_11 |
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