HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 273797Generated: October 30, 2026
Ethyl orthoformate → 5-(Chloromethyl)-9-methyl-1,2,4-triazolo[4,3-c]quinazoline
https://huagongshe.com/reaction/273797
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl orthoformate | HCID 31214 | — |
| Reactant | 2-(Chloromethyl)-4-hydrazino-6-methylquinazoline | HCID 20094053 | — |
| Product | 5-(Chloromethyl)-9-methyl-1,2,4-triazolo[4,3-c]quinazoline | HCID 20094106 | — |
Reaction Steps
4. 58.2 g of 2-(chloromethyl)-4-hydrazino-6-methylquinazoline in 870 ml of triethyl orthoformate are heated to reflux temperature while stirring in an oil bath pre-heated to 100° C. and stirred at this temperature for a further 0.5 h. (bath temperature 140°-145° C.). About 40 ml of ethanol are distilled off during the heating. Thereafter, the mixture is concentrated in a vacuum to a volume of about 150 ml. 150 ml of diethyl ether are then added thereto, the mixture is cooled to 0° to 5° C. and the crystals are filtered off. The product is washed with ethanol/diethyl ether 1:2 and with diethyl ether and dried in a vacuum. 55.1 g of crude 5-(chloro-methyl)-9-methyl-1,2,4-triazolo[4,3-c]quinazoline of m.p. 175° C. are obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05387585 |
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| Source dataset | uspto-grants-1995_02 |
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| ORD ID | ord-2ab04f77446c4da49c2085019344ef82 |
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| Source note | uspto-grants-1995_02 |
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