HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 44423Generated: October 25, 2026
Ethyl chloroacetate → ethyl 2-(1-methyl-2,6-dioxo-2,3-dihydro-1H-purin-7(6H)-yl)acetate
https://huagongshe.com/reaction/44423
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl chloroacetate | HCID 7751 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1-Methylxanthine | HCID 80220 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | ethyl 2-(1-methyl-2,6-dioxo-2,3-dihydro-1H-purin-7(6H)-yl)acetate | HCID 59205119 | 79.3% |
Reaction Steps
To a solution of 1-methyl xanthine (120, 1 g, 6.01 mmol) in DMF, potassium carbonate (0.91 g, 6.6 mmol) was added and the reaction mixture was heated to 90° C. and stirred for 1 h. A solution of ClCH2COOEt (0.36 g, 3.0 mmol) in DMF was then added dropwise to the reaction over 45 min. After stirring an additional 15 min, the reaction was cooled to room temperature and poured into ice cold 1N HCl (50 ml). The reaction was then extracted with chloroform (50×2 ml). The combined organic layers were washed with water (100 mL), dried over Na2SO4 and concentrated in vacuo. To the resulting solid was added 30% dichloromethane in hexanes (400 mL) and the resulting mixture was stirred for 15 min and filtered to yield compound 121 as a yellow solid (0.6 g, 40%). MS (APCI): m/z 253.32 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08541423B2 |
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| Source dataset | uspto-grants-2013_09 |
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| ORD ID | ord-200931c65fca4fc7b4b5168e2dea6933 |
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| Source note | uspto-grants-2013_09 |
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