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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300895Generated: October 31, 2026

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

https://huagongshe.com/reaction/2300895

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Bromopyridinium chlorideHCID 88100—
Reactant2-[(S)-1-phenylethylamino]-4-[5-aminobenzimidazol-1-yl]pyrimidineHCID 9883977—
SolventDimethylformamideHCID 6228—
Product2-[(S)-1-phenylethylamino]-4-[5-(pyridin-4-yl)aminobenzimidazol-1-yl]pyrimidineHCID 599248868.1%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-[(S)-1-phenylethylamino]-4-[5-aminobenzimidazol-1-yl]pyrimidine (49.8 mg) was dissolved in DMF (2 mL). Diisopropylethylamine (79 μL) and 4-bromopyridine hydrochloride (43.2 mg) were added, and the mixture left heating overnight at 100° C. After 17 h added more diisopropylethylamine (79 μL) and 4-bromopyridine hydrochloride (40.2 mg) and continued heating at 100° C. for another 24 h. The volatiles were removed in vacuo and the residue purified on silica gel (2-5%(2M NH3 in MeOH)/CH2Cl2) to yield 5.0 mg of impure product that was purified by HPLC (Zorbax Rx-SIL, 60:40 hexanes:ethanol) to yield 3.0 mg of the title compound. Mass spectrum (ESI) 408.4 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498165B1
Source datasetuspto-grants-2002_12
ORD IDord-a1c10b40483c4f658deebc2f605d02ee
Source noteuspto-grants-2002_12