HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244459Generated: October 29, 2026
Dimethylformamide → 5-Allyl-3-methyl-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one
https://huagongshe.com/reaction/244459
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-allyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidine | HCID 59437321 | — |
| Solvent | Water | HCID 962 | — |
| Product | 5-Allyl-3-methyl-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one | HCID 59437277 | 64% |
Reaction Steps
To a room temperature solution of 5-allyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidine (220 mg, 1.3 mmol, 1 equiv.) in 3 mL of DMF was added 60% NaH (100 mg, 2.5 mmol, 2 equiv.) followed by MeI (0.18 ml, 1.8 mmol, 1.5 equiv.). After 30 minutes, the mixture was diluted with water and extracted with EtOAc. The combined organic layers were dried, filtered, and concentrated in vacuo. The residue was purified by reverse phase HPLC (5-90% CH3CN/water+0.1% TFA). The desired fractions were combined and concentrated to remove CH3CN. The remaining aqueous mixture was extracted with EtOAc, dried, filtered, and evaporated to provide 152 mg (64%) of 5-allyl-3-methyl-3,5-dihydropyrrolo[3,2-d]pyrimidin-4-one as a yellow oil which was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08658637B2 |
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| Source dataset | uspto-grants-2014_02 |
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| ORD ID | ord-7b18bbcdd92f4a0c9ff57180fd1089fb |
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| Source note | uspto-grants-2014_02 |
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