HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1926116Generated: November 2, 2026
Water → 2-[2-(6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoate
https://huagongshe.com/reaction/1926116
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine | HCID 56851055 | — |
| Reactant | 2-{2-[(Methylsulfonyl)oxy]ethoxy}ethyl benzoate | HCID 86615775 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-[2-(6-methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidin-5-yl)ethoxy]ethyl benzoate | HCID 56851056 | 93.2% |
Reaction Steps
6-Methyl-4-phenoxy-5H-pyrrolo[3,2-d]pyrimidine (299.9 mg) and 2-{2-[(methylsulfonyl)oxy]ethoxy}ethyl benzoate (464.1 mg) were dissolved in N,N-dimethylformamide (7 mL), potassium carbonate (431 mg) was added, and the mixture was stirred at 60° C. for 21 hr. Water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine, dried over anhydrous magnesium sulfate and concentrated under reduced pressure. The residue was separated and purified by silica gel column chromatography (eluent, hexane:ethyl acetate=80:20→20:80) to give the title compound (517.8 mg) as a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08178543B2 |
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| Source dataset | uspto-grants-2012_05 |
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| ORD ID | ord-722967ff98684ac6bab65646ac8eb962 |
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| Source note | uspto-grants-2012_05 |
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