HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 981205Generated: October 31, 2026
3-Amino-1,2,4-triazine → HCID 20071616, compound
https://huagongshe.com/reaction/981205
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 3-Amino-1,2,4-triazine | HCID 70715 | — |
| Reactant | Ethyl 2-(2,7-dichloro-6-fluoroquinoline-3-carbonyl)-3-dimethylaminoacrylate | HCID 54015905 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | HCID 20071616 | HCID 20071616 | 64.8% |
Reaction Steps
A mixture of 11.3 g of ethyl 2-(2,7-dichloro-6-fluoroquinoline-3-carbonyl)-3-dimethylaminoacrylate and 5.65 g of 3-amino-1,2,4-triazine in 60 cm3 of trichloromethane is stirred for 16 hours at a temperature close to 20° C. The reaction mixture is concentrated to dryness under reduced pressure (20 kPa) at a temperature close to 30° C. The residue is taken up in 60 cm3 of ethanol and 5.6 g of DBU and the mixture is heated at a temperature close to 75° C. for 20 hours. After cooling to 20° C., the insoluble matter is drained and washed with twice 40 cm3 of ethanol. 6.1 g of 8-chloro-3-ethoxycarbonyl-7-fluoro-4-oxo-1,4-dihydro-benzo[b][1,8]naphthyridine are obtained in the form of a brown solid which decomposes at 378°-380° C. and is used for the subsequent steps without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04990515 |
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| Source dataset | uspto-grants-1991_02 |
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| ORD ID | ord-5b286fba610e4c62b6fbeda5a94f2019 |
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| Source note | uspto-grants-1991_02 |
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