HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1786932Generated: October 29, 2026
Phosphorus oxychloride → 4-chloro-6-(furan-2-yl)-5H-pyrrolo[3,2-d]pyrimidine
https://huagongshe.com/reaction/1786932
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | 6-(furan-2-yl)-5H-pyrrolo[3,2-d]pyrimidin-4-ol | HCID 135741775 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 4-chloro-6-(furan-2-yl)-5H-pyrrolo[3,2-d]pyrimidine | HCID 71303347 | 91.2% |
Reaction Steps
A mixture of 6-(2-furyl)-4,5-dihydro-3H-pyrrolo[3,2-d]pyrimidin-4-one (2.20 g) and phosphoryl chloride (10.7 g) was stirred at 100° C. for 20 min, dioxane (30 mL) was added, and the mixture was stirred at 100° C. for 3 hrs. After concentration under reduced pressure, saturated aqueous sodium hydrogen carbonate was added to the residue, and the mixture was extracted with ethyl acetate-acetone (155 mL×4). The organic layers were combined, washed with saturated brine (100 mL), dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The residue washed with ethyl acetate-diethyl ether, and dried under reduced pressure at 60° C. to give the title compound (2.19 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07507740B2 |
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| Source dataset | uspto-grants-2009_03 |
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| ORD ID | ord-60364eed59cf42df9902b300bf8ffe2b |
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| Source note | uspto-grants-2009_03 |
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