HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502650Generated: October 31, 2026
2-Pyridinamine, 5-iodo- → HCID 77985005, compound
https://huagongshe.com/reaction/1502650
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Pyridinamine, 5-iodo- | HCID 88579 | — |
| Reactant | HCID 86717668 | HCID 86717668 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 77985005 | HCID 77985005 | 70.7% |
Reaction Steps
657 mg (corresponding to 2.46 mmol) of 5-(2-bromoacetyl)-2-(1H-1,2,4-triazole-1-yl)pyridine and 541 mg (corresponding to 2.46 mmol) of 2-amino-5-iodopyridine were dissolved in 5.0 mL of acetonitrile. The resulting solution was heated under reflux for 1.5 hours in an oil bath at 100° C. After the completion of the reaction, the reaction solution was cooled down to room temperature, and precipitates were filtered. The precipitates were washed with acetonitrile and dried under reduced pressure. The resulting crude crystals were suspended in a mixed solution of 2 mL of water and 2 mL of methanol. Then, about 1 mL of a saturated sodium hydrogencarbonate solution was added thereto, and the mixture was sonicated for 10 minutes using an ultrasonic washing machine. Precipitates were filtered and recovered from the resulting mixture, sufficiently washed with water, and dried under reduced pressure, to obtain 675 mg (corresponding to 1.74 mmol) of 6-iodo-2-[2-(1H-1,2,4-triazole-1-yl)pyridine-5-yl]imidazo[1,2-a]pyridine (FIG. 4, step 3).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09211350B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-4035f551d69e4e7ba8aa75827ec4773b |
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| Source note | uspto-grants-2015_12 |
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