HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl bromoacetate → (2-Amino-6-iodopurin-9-yl)-acetic acid ethyl ester
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl bromoacetate | HCID 7748 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Amino-6-iodopurine | HCID 6101575 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | (2-Amino-6-iodopurin-9-yl)-acetic acid ethyl ester | HCID 85849531 | 95% |
Reaction Steps
To a solution of 2-amino-6-iodo-purine (78.3 g, 0.3 mol) in DMF (1960 mL) was added ethyl bromoacetate (55.1 g, 0.33 mol) and potassium carbonate (82.9 g, 0.6 mol). The resulting reaction mixture was stirred for 12 h at room temperature. The reaction mixture was concentrated to small volume (about 150 mL) in vacuo and the residue was dissolved in water. The solid was filtered off, washed with water and ethyl ether, and dried in vacuo to give the titled compound (98.4 g, 95%). 1H-NMR (500 MHz; DMSO-d6) δ 8.06 (s, 1H), 6.90 (br.s, 2H), 4.94 (s, 2H), 4.17 (q, 2H), 1.22 (t, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07179896B2 |
| Source dataset | uspto-grants-2007_02 |
| ORD ID | ord-eaa9194d6ff0453c91e790226098617c |
| Source note | uspto-grants-2007_02 |