HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1502644Generated: October 31, 2026
2-Pyridinamine, 5-iodo- → HCID 77985004, compound
https://huagongshe.com/reaction/1502644
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Pyridinamine, 5-iodo- | HCID 88579 | — |
| Reactant | HCID 86717667 | HCID 86717667 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 77985004 | HCID 77985004 | 35.3% |
Reaction Steps
20.4 mg (corresponding to 0.0764 mmol) of 5-(2-bromoacetyl)-2-(2H-1,2,3-triazole-2-yl)pyridine and 16.8 mg (corresponding to 0.0764 mmol) of 2-amino-5-iodopyridine were dissolved in 2.0 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 10.4 mg (corresponding to 0.027 mmol) of 6-iodo-2-[2-(2H-1,2,3-triazole-2-yl)pyridine-5-yl]imidazo[1,2-a]pyridine (FIG. 2, 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-f15bdb7cb6d2453788b0b8790481a844 |
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| Source note | uspto-grants-2015_12 |
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