HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1485514Generated: October 27, 2026
Phosphorus oxychloride → 4,6-Dichloropyrido[3,2-d]pyrimidine
https://huagongshe.com/reaction/1485514
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-chloro-1H-pyrido[3,2-d]pyrimidin-4-one | HCID 178518217 | — |
| Product | 4,6-Dichloropyrido[3,2-d]pyrimidine | HCID 10584165 | 73% |
Reaction Steps
To a solution of 6-chloropyrido[3,2-d]pyrimidin-4(1H)-one (150 mg, 0.83 mmol) in POCl3 (2.0 mL) was added DIPEA (0.22 mL, 1.24 mmol) at room temperature. After stirring for 1 hour at 110° C., the reaction mixture was cooled to room temperature. The reaction mixture was concentrated in vacuo, and then diluted with water and extracted with dichlormethane. The combined organic layers were washed brine, dried over anhydrous Na2SO4, filtered and concentrated in vacuo. The residue was purified by column chromatography on SiO2 (Hex:EtOAc=10:1) to give 4,6-dichloropyrido[3,2-d]pyrimidine (120 mg, 73%) as a yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 7.87 (1H, d, J=8.8 Hz), 8.35 (1H, d, J=8.8 Hz), 9.14 (1H, s).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09422298B2 |
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| Source dataset | uspto-grants-2016_08 |
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| ORD ID | ord-770ad2b97421482192674867d82c2f36 |
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| Source note | uspto-grants-2016_08 |
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