HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 728029Generated: October 29, 2026
Hydrochloric Acid → 3-Methylthio-8-oxo-6-(2-methoxyphenyl)-7,8-dihydropyrimido[4,5-e][1,2,4]triazine
https://huagongshe.com/reaction/728029
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methoxy-benzamidine | HCID 4321834 | — |
| Reactant | Ethyl 5-Chloro-3-(Methylthio)-1,2,4-Triazine-6-Carboxylate | HCID 11557703 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 3-Methylthio-8-oxo-6-(2-methoxyphenyl)-7,8-dihydropyrimido[4,5-e][1,2,4]triazine | HCID 135670785 | — |
Reaction Steps
A cooled (0° C.) solution of 2-methoxybenzamidine (from 1.97 g of the hydrochloride) in acetonitrile (17 ml) was added to a cooled solution of 3-methylthio-5-chloro-6-carboethoxy-1,2,4-triazine (prepared from 3-methylthio-5-oxo-6-carboethoxy-4,5-dihydro-1,2,4-triazine, 1.08 g, and thionyl chloride, 20 ml) in acetonitrile (17 ml). Triethylamine (0.51 g) was added and the reaction mixture was stirred with cooling (0° C.) for one hour and then at ambient temperature for 17 hours to afford a yellow solid which was washed with acetonitrile and ether to afford the crude title compound (1.39 g). A sample (0.35 g) of this was washed twice with boiling methanol to afford the title compound, 0.25 g, m.p. 267.5°-268.5° C. The remaining material (1.04 g) was similarly treated with boiling methanol to afford the title compound, 0.91 g, m.p. 266°-268° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05047404 |
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| Source dataset | uspto-grants-1991_09 |
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| ORD ID | ord-3c00af590a2c403dbbd1649498e33327 |
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| Source note | uspto-grants-1991_09 |
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