HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582991Generated: October 31, 2026
Diisopropylethylamine → HCID 178462948, compound
https://huagongshe.com/reaction/1582991
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | Pyrazole-1-carboxamidine monohydrochloride | HCID 2734672 | — |
| Reactant | HCID 12991183 | HCID 12991183 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 178462948 | HCID 178462948 | 172.4% |
Reaction Steps
To a 15 ml 1,4-dioxane solution containing 314 mg of 3-(2-aminoethyl)-4-(3-chlorophenyl)-1-ethyl-7-methyl-1,8-naphthyridin-2(1H)-one were added 404 mg of 1-amidinopyrazole monohydrochloride and 0.48 ml of diisopropylethylamine, followed by stirring for 122 hours. The reaction solution was evaporated, the resulting solid was removed by filtration, and the solid was further washed with chloroform. The combine filtrate and washings were concentrated and the residue was purified by a silica gel column chromatography (chloroform-methanol-aqueous ammonia). The resulting oily substance was dissolved in 5 ml of ethanol, and 0.5 ml of 4M hydrogen chloride-ethyl acetate and acetonitrile were added thereto successively. The solvent was evaporated to obtain 347 mg of 4-(3-chlorophenyl)-1-ethyl-3-(2-guanidinoethyl)-7-methyl-1,8-naphthyridin-2(1H)-one monohydrochloride monohydrate as a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06740662B1 |
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| Source dataset | uspto-grants-2004_05 |
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| ORD ID | ord-74e02a9fb3b04254b86fcd51cde21eca |
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| Source note | uspto-grants-2004_05 |
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