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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 8157Generated: October 26, 2026

Pyridine → 5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzene

https://huagongshe.com/reaction/8157

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantBenzyl chloroformateHCID 10387—
ReactantSodium BicarbonateHCID 516892—
Reactant3-Fluoro-4-(4-methyl-1H-imidazol-1-yl)anilineHCID 21876638—
SolventDichloromethaneHCID 6344—
Product5-Benzyloxycarbonylamino-2-(4-methylimidazol-1-yl)fluorobenzeneHCID 2187667292.9%

Reaction Steps

5-Amino-2-(4-methylimidazol-1-yl)fluorobenzene (50.6 g, 0.265 M) was dissolved in dry dichloromethane (800 ml) under nitrogen, and cooled to −5°. Pyridine (26.1 g, 0.33 M) was added, followed by benzyl chloroformate (49.9 g, 0.292 M) over 30 minutes. The mixture was stirred and the temperature allowed to rise to ambient over 16 hours. Aqueous sodium bicarbonate (5%, 350 ml) was added, the organic layer separated, and the aqueous layer re-extracted with dichloromethane (2×200 ml), and combined organics dried (magnesium sulfate). After filtration and evaporation, the residue was recrystallised from toluene (300 ml) to give title product (80 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07087629B2
Source datasetuspto-grants-2006_08
ORD IDord-f57646be41af44fcb4ffc0a07957ff78
Source noteuspto-grants-2006_08