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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 899685Generated: October 29, 2026

1H-imidazole-2-carbaldehyde → HCID 62222276, compound

https://huagongshe.com/reaction/899685

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-imidazole-2-carbaldehydeHCID 24955—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Bromomethyl)pyridine hydrobromideHCID 2734720—
SolventDimethylformamideHCID 6228—
ProductHCID 62222276HCID 6222227637.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of the 2-imidazolecarboxaldehyde (545 mg, 5.67 mmol) and 2-(bromomethyl)pyridine hydrobromide (1.58 g, 6.24 mmol) in DMF (20 mL) was added N,N-diisopropylethylamine (3.0 mL, 17.01 mmol). The reaction mixture was heated to 80° C. overnight. Then it was cooled and quenched with saturated NaHCO3 (20 mL). It was extracted with CH2Cl2 (c×20 mL). The combined organic layers were washed with brine (20 mL), dried (MgSO4), filtered, concentrated, and dried in vacuo to afford a dark brown oil. Purification by flash column chromatography on silica gel using 1%→2% CH3OH/CH2Cl2 afforded the product as a yellow solid (397 mg, 37%). 1H NMR (CDCl3) δ 5.71 (s, 2H), 7.18-7.24 (m, 2H), 7.32 (s, 1H), 7.36 (s, 1H), 7.65 (td, 1H, J=10.4, 1.5 Hz), 8.56 (d, 1H, J=4.5 Hz), 9.82 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07354932B2
Source datasetuspto-grants-2008_04
ORD IDord-4e6ebc77cd5b4ea2b8f7aa1024c938ed
Source noteuspto-grants-2008_04