HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2404072Generated: October 30, 2026
Chloroacetaldehyde → Imidazo[1,2-a]pyridine-8-carbonitrile
https://huagongshe.com/reaction/2404072
Participants
| Role | Name | HCID | Charge |
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| Reactant | Chloroacetaldehyde | HCID 33 | — |
| Reactant | 2-Amino-3-cyanopyridine | HCID 818259 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | Imidazo[1,2-a]pyridine-8-carbonitrile | HCID 15098893 | 100% |
Reaction Steps
To a solution of 2-aminonicotinonitrile (1.0 g, 8.39 mmol) in EtOH (10 ml) in a 20 ml sealed vial was added 2-chloroacetaldehyde (1.611 ml, 9.23 mmol) vial was then sealed and heated to 120° C. overnight. Reaction was cooled to RT and quenched with 2N Na2CO3, removed EtOH in vaccuo and extracted with DCM×3. Combined organics and washed with water then brine×2. Dired over sodium sulfate and removed solvent to give title compound as a yellow brown solid (1.2 g, 8.38 mmol, 100% yield) was verified by MS (ES+) C8H5N3 requires: 143 found: 144 [M+H]+
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08802697B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-1bd9264344a44af1b269ac1b19efff43 |
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| Source note | uspto-grants-2014_08 |
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