HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 972716Generated: October 29, 2026
Methanol → 5,8,9-Trimethoxy-1,2,4-triazolo-[4,3-c]quinazoline
https://huagongshe.com/reaction/972716
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 5-Chloro-8,9-dimethoxy-1,2,4-triazolo[4,3-c]quinazoline | HCID 21405143 | — |
| Product | 5,8,9-Trimethoxy-1,2,4-triazolo-[4,3-c]quinazoline | HCID 21405146 | — |
Reaction Steps
A mixture of 500 mg 5-chloro-8,9-dimethoxy-1,2,4-triazolo[4,3-c]quinazoline and 25 ml triethylamine in 25 ml. methanol is stirred at 40° C. for 24 hrs. The solution is then evaporated in vacuo to dryness, treated with water, and the aqueous layer extracted several times with chloroform. The combined chloroform extracts, after washing with H2O, is dried over sodium sulfate and evaporated in vacuo to dryness. The residue is dissolved in minimum chloroform and chromotrographed on silica gel, elution being carried out with chloroform and then with chloroform containing increasing concentrations of methanol. The desired fractions are collected, evaporated to dryness in vacuo and the residue crystallized from methylene chloride/diethyl ether to obtain 5,8,9-Trimethoxy-1,2,4-triazolo-[4,3-c]quinazoline, m.p. 245°-250° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04053600 |
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| Source dataset | uspto-grants-1977_10 |
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| ORD ID | ord-63c193772c0342f793eff0a6e9486e9c |
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| Source note | uspto-grants-1977_10 |
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