HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 530111Generated: October 30, 2026
Triethylamine → 2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one
https://huagongshe.com/reaction/530111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-chloro-7-methyl-8-phenyl-7,8-dihydropteridin-6(5H)-one | HCID 89560835 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-chloro-7-methyl-5,8-diphenyl-7,8-dihydropteridin-6(5H)-one | HCID 89570391 | 37% |
Reaction Steps
To a stirred solution of 2-chloro-7-methyl-8-phenyl-7,8-dihydropteridin-6(5H)-one (1.59 g, 5.78 mmol) in dichloromethane (75 mL) was added triethylamine (8.07 ml, 57.8 mmol), cupric acetate (2.09 g, 11.56 mmol) and phenylboronic acid (1.41 g, 11.56 mmol) followed by 4 Å molecular sieves (2 g). The resulting mixture was stirred for 48 h at rt with an air balloon on the top. The reaction mixture was then filtered over celite to give a clear solution. The solution was washed with aqueous saturated sodium bicarbonate (50 mL×2), dried over anhydrous sodium sulfate and evaporated to give a crude material, which was then purified by silica gel column chromatography (eluent: 2% methanol in dichloromethane) to give the desired product (750 mg, 37%). 1HNMR (300 MHz, CDCl3): δ 1.65 (d, J=6.9 Hz, 3H), 4.82 (q, J=6.9 Hz, 1H) and 7.36-7.65 (m, 11H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09351974B2 |
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| Source dataset | uspto-grants-2016_05 |
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| ORD ID | ord-080b5a100755434693f4e915db85f75c |
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| Source note | uspto-grants-2016_05 |
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