Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Ethyl Bromide | HCID 6332 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 135556678 | HCID 135556678 | — |
| Product | HCID 22386542 | HCID 22386542 | 36% |
Reaction Steps
To 4-(5-Ethylsulfanyl-imidazo[1,2-c]pyrimidin-7-yl)-benzene-1,2-diol (86.2 mg, 0.3 mmol) in DMF (2 ml) were added ethyl bromide (112 μl, 1.5 mmol) and K2CO3 (290 mg, 2.1 mmol). The reaction mixture was stirred at about 50° C. overnight. After cooling to room temperature, it was poured into water and extracted with EtOAc. The combined organic extract was dried over MgSO4 and concentrated in vacuo. The residue was purified by preparative thin layer chromatography to give 7-(3,4-Diethoxy-phenyl)-5-ethylsulfanyl-imidazo[1,2-c]pyrimidine (39.1 mg, yield 36%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06911443B2 |
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| Source dataset | uspto-grants-2005_06 |
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| ORD ID | ord-3466614857ef4df69b05df68f51af4ca |
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| Source note | uspto-grants-2005_06 |
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