HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 60132Generated: October 29, 2026
tert-Butanol → HCID 67774787, compound
https://huagongshe.com/reaction/60132
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butanol | HCID 6386 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Diphenylphosphate azide | HCID 21964642 | — |
| Reactant | 2-Bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate | HCID 131732575 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67774787 | HCID 67774787 | — |
Reaction Steps
Triethylamine (0.39 ml), MS4A (1.5 g), and diphenyl phosphate azide (0.18 ml) were added to a tert-butanol (5 ml) solution of the 2-bromo-[1,2,4]triazolo[1,5-a]pyridine-7-carboxylate (0.17 g) obtained in (Example 3.15) <Step 3>. The obtained mixture was stirred at room temperature for 1 hour, and then at 100° C. for 2 hours. Thereafter, ethyl acetate (50 ml) was added to the reaction solution, and the mixed solution was then filtered with Celite. The filtrate was washed with a saturated sodium hydrogen carbonate aqueous solution (20 ml), and was then dried over anhydrous sodium sulfate. The solvent was distilled away under reduced pressure, and the obtained residue was then purified by silica gel column chromatography (silica gel:eluent; heptane:ethyl acetate=75:25-50:50), so as to obtain the title compound (0.15 g) in a white amorphous form.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440970B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-8520afef55394953ae653d2f830087d7 |
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| Source note | uspto-grants-2016_09 |
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