HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796095Generated: November 3, 2026
HCID 69560024, compound → HCID 10292909, compound
https://huagongshe.com/reaction/1796095
Participants
| Role | Name | HCID | Charge |
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| Reactant | HCID 69560024 | HCID 69560024 | — |
| Catalyst | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 10292909 | HCID 10292909 | 28% |
Reaction Steps
7-(1-Methyl-1-triethylsilanyloxyethyl)-3-[2-(3-nitrophenyl)-pyrimidin-4-yl]imidazo[1,2-α]pyrimidine in EtOH (10 ml) was treated with conc. HCl (10 drops) and stirred at room temperature for 12 h. The crude mixture was poured onto an SCX cartridge (2 gram) and washed firstly with MeOH (20 ml) to remove the impurities and then 2N NH3 in MeOH (20 ml) to elute the desired compound. Removal of the solvent under reduced pressure afforded 2-{3-[2-(3-nitrophenyl)pyrimidin-4-yl]imidazo[1,2-α]pyrimidin-7-yl}propan-2-ol (66 mg, 28%): 1H NMR (360 MHz, CDCl3) δ 10.31 (1H, d, J 7.3), 9.31 (1H, t, J 1.8), 8.83 (1H, d, J 5.5), 8.80 (1H, d, J 8.0), 8.55 (1H, s), 8.40 (1H, d, J 8.0), 7.75 (1H, t, J 8.0), 7.66 (1H, d, J 5.5), 7.40 (1H, d, J 7.3), 1.68 (6H, s); m/z (ES+) 377 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07030128B2 |
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| Source dataset | uspto-grants-2006_04 |
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| ORD ID | ord-47f0d5b6b5eb4d408b6ae1eda8cbd526 |
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| Source note | uspto-grants-2006_04 |
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