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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300894Generated: October 31, 2026

2-[(S)-1-phenylethylamino]-4-[5-aminobenzimidazol-1-yl]pyrimidine → 2-[(S)-1-phenylethylamino]-4-[5-(pyrimidin-4-yl)aminobenzimidazol-1-yl]pyrimidine

https://huagongshe.com/reaction/2300894

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-[(S)-1-phenylethylamino]-4-[5-aminobenzimidazol-1-yl]pyrimidineHCID 9883977—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
Product2-[(S)-1-phenylethylamino]-4-[5-(pyrimidin-4-yl)aminobenzimidazol-1-yl]pyrimidineHCID 990937763.6%

Reaction Steps

2-[(S)-1-phenylethylamino]-4-[5-aminobenzimidazol-1-yl]pyrimidine (14.0 mg) was dissolved in 2 mL MeOH, 10%Pd/C (20.3 mg) added, the system fitted with a balloon of hydrogen, purging the system twice and leaving the reaction stirring at room temperature for 23 h. The mixture was then filtered through Celite®, washing thoroughly with methanol, and the solvent removed in vacuo. The residue was purified on silica gel (2-5%(2M NH3 in MeOH)/CH2Cl2) to yield 5.5 mg of the title compound. Mass spectrum (ESI) 409.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498165B1
Source datasetuspto-grants-2002_12
ORD IDord-ec468ceaac1e48b9923c33120aaac479
Source noteuspto-grants-2002_12