HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588430Generated: October 30, 2026
Bromoform → 2,6-Dibromo-[1,2,4]triazolo[1,5-a]pyridine
https://huagongshe.com/reaction/588430
Participants
| Role | Name | HCID | Charge |
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| Reactant | Bromoform | HCID 5558 | — |
| Reactant | Dichloroacetic Acid | HCID 6597 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 6-Bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine | HCID 25215940 | — |
| Catalyst | Benzyltriethylammonium bromide | HCID 165294 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2,6-Dibromo-[1,2,4]triazolo[1,5-a]pyridine | HCID 68390875 | 26% |
Reaction Steps
A mixture of 6-bromo-[1,2,4]triazolo[1,5-a]pyridin-2-amine (20.86 g, 97.9 mmol), sodium nitrite (67.6 g, 979 mmol) and benzyltriethylammonium bromide (53.3 g, 196 mmol) in bromoform (1.47 kg, 508 ml, 5.81 mol) was stirred for 30 minutes at 25° C. Then dichloroacetic acid (25.3 g, 16.2 ml, 196 mmol) was added and the mixture was stirred for 20 hours at 25° C. under exclusion of light. 600 ml of water were added to the mixture and stirred for 30 minutes. The mixture was diluted with water and dichloromethane, filtrated over dicalite and the filtrate extracted 3 times with dichloromethane. The organic layers were combined, washed with water, dried over magnesium sulfate, filtrated and evaporated to dryness under reduced pressure. The crude material was purified by flash chromatography in 2 portions over 2×70 g silica columns using dichloromethane/methanol 5% as eluent, affording 2,6-dibromo-[1,2,4]triazolo[1,5-a]pyridine (7 g, 26%) as light brown solid. Mp.: 201° C. MS: m/z=277.7/279.9 (M+H+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227970B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-94c6245194c640c188bc6ddf01a52fa9 |
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| Source note | uspto-grants-2016_01 |
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