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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2300884Generated: November 2, 2026

Sodium hydride → HCID 59924884, compound

https://huagongshe.com/reaction/2300884

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium hydrideHCID 24758—
ReactantHCID 18375727HCID 18375727—
ReactantHCID 59924895HCID 59924895—
SolventDimethylformamideHCID 6228—
SolventSodium BicarbonateHCID 516892—
ProductHCID 59924884HCID 5992488448.6%

Reaction Conditions

Temperature80 °C

Reaction Steps

2-[(S)-1-Phenylethylamino]-4-[5-hydroxybenzimidazol-1-yl]-pyrimidine (25 mg) was dissolved in DMF (2.0 mL) and NaH (60%, 6.0 mg) was added followed by N-benzyloxycarbonyl-2-(methanesulfonyloxy)methylpyrrolidine (20 mg) and the resulting suspension was heated to 80° C. for 1 hour. After cooling to room temperature, the solution was then diluted with 10 mL of aqueous saturated NaHCO3 and extracted with 2×10 mL of of EtOAc. The combined organic extracts were then dried (MgSO4) and concentrated under reduced pressure. The residue was purified with preparative thin-layer chromatography (SiO2, 5% MeOH in CH2Cl2) to yield 17 mg of 2-[(S)-1-Phenylethylamino]-4-[5-((N-benzyloxycarbonyl-pyrrolidin-2-yl)methoxy)benzimidazol-1-yl]pyrimidine. Mass spectrum (ESI) 549.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06498165B1
Source datasetuspto-grants-2002_12
ORD IDord-02de94712e694780a6b6b67e94a82f7b
Source noteuspto-grants-2002_12