HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 659176Generated: October 30, 2026
tert-Butyl methyl ether → HCID 54766016, compound
https://huagongshe.com/reaction/659176
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | tert-Butyl methyl ether | HCID 15413 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-(6-Methylpyridin-2-yl)-2-([1,2,4]triazolo[1,5-a]pyridin-6-yl)ethane-1,2-dione | HCID 51051644 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 54766016 | HCID 54766016 | 33% |
Reaction Steps
To a stirred solution of 1-((1,2,4)triazolo(1,5-a)pyridin-6-yl)-2-(6-methylpyridin-2-yl)ethane-1,2-dione (4.00 g, 15.02 mmol) in a mixture of tert-butyl methyl ether (30 mL) and MeOH (30 mL) were added 3-(fomylmethyl)benzonitrile (prepared according to the method described in WO 02/096875 A1) (6.54 g, 45.07 mmol) and NH4OAc (11.58 g, 150.24 mmol), and the mixture was stirred at room temperature for 90 min. The pH of the mixture was adjusted to 8 with saturated aqueous NaHCO3 solution. After removal of solvent, the mixture was extracted with EtOAc (2×150 mL), and the EtOAc solution was washed with water (50 mL) and brine (50 mL), dried over anhydrous Na2SO4, filtered, and evaporated to dryness under reduced pressure. The residue was purified by MPLC on silica gel using a mixture of MeOH and CH2Cl2 (1:19 (v/v)) as eluent to give the titled compound (1.92 g, 33%) as a yellow solid. 1H NMR (400 MHz, DMSO-d6) δ 12.70 (br s, 1H), 9.53 (br s, 1H), 8.49 (s, 1H), 7.96 (dd, 1H, J=9.2, 1.8 Hz), 7.84 (d, 1H, J=2.0 Hz), 7.82 (d, 1H, J=9.2 Hz), 7.74-7.71 (m, 2H), 7.69 (t, 1H, overlapped, J=7.6 Hz), 7.56 (t, 1H, J=7.8 Hz), 7.47 (br s, 1H), 7.15 (d, 1H, J=7.6 Hz), 4.18 (s, 2H), 2.47 (s, 3H); MS (ESI) m/z 392.18 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08080568B1 |
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| Source dataset | uspto-grants-2011_12 |
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| ORD ID | ord-f857c109d55a4ee88b068e7eec9298c2 |
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| Source note | uspto-grants-2011_12 |
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