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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1796095Generated: November 3, 2026

HCID 69560024, compound → HCID 10292909, compound

https://huagongshe.com/reaction/1796095

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 69560024HCID 69560024—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 10292909HCID 1029290928%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07030128B2
Source datasetuspto-grants-2006_04
ORD IDord-47f0d5b6b5eb4d408b6ae1eda8cbd526
Source noteuspto-grants-2006_04