HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1516839Generated: October 27, 2026
2,4,6-Trimethylphenol → 5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-amine
https://huagongshe.com/reaction/1516839
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2,4,6-Trimethylphenol | HCID 10698 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine | HCID 57693617 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | 5-benzyl-4-(mesityloxy)-5H-pyrrolo[3,2-d]pyrimidin-2-amine | HCID 57693662 | 50.1% |
Reaction Steps
To a stirred suspension of NaH (56 mg, 2.33 mmol) in dry NMP (2 mL) was added 2,4,6-trimethyl phenol (317 mg, 2.33 mmol). The mixture was stirred at room temperature for 30 min under argon. The reaction mixture was added to a solution of 5-benzyl-4-chloro-5H-pyrrolo[3,2-d]pyrimidin-2-amine (200 mg, 0.78 mmol) in dry NMP (1.5 mL) and the resulting solution was heated at 90° C. for 16 h. After completion of the reaction, the reaction mixture was diluted with water and washed with EtOAc. The combined organic layers were washed with water, 2% NaOH, and brine and dried over Na2SO4, filtered, and concentrated in vacuo. The crude product was purified by column chromatography, eluting with hexanes/ethyl acetate (3:1) to give the product as a white solid (140 mg, 50%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08227601B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-3c576f605b2b4a1e9240eac56eab6a07 |
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| Source note | uspto-grants-2012_07 |
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