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
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-(Bromomethyl)pyridine hydrobromide | HCID 2734720 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 62222276 | HCID 62222276 | 37.4% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07354932B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-4e6ebc77cd5b4ea2b8f7aa1024c938ed |
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| Source note | uspto-grants-2008_04 |
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