HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 484858Generated: October 25, 2026
Carbon Dioxide → 3-{[3-(Diethylamino)propyl]amino}-1,2-dihydro-4H-indazol-4-one
https://huagongshe.com/reaction/484858
Participants
| Role | Name | HCID | Charge |
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| Reactant | Carbon Dioxide | HCID 280 | — |
| Reactant | Oxygen | HCID 977 | — |
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | 2-Bromopropane | HCID 6358 | — |
| Reactant | Magnesium | HCID 5462224 | — |
| Reactant | 1,3-Propanediamine,n3-(4-chloro-1h-indazol-3-yl)-n1,n1-diethyl- | HCID 20135847 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Diethyl Ether | HCID 3283 | — |
| Product | 3-{[3-(Diethylamino)propyl]amino}-1,2-dihydro-4H-indazol-4-one | HCID 135583100 | 41% |
Reaction Steps
To 20 ml of diethyl ether solution containing 600 mg of magnesium powder was added dropwise a mixed solution consisting of 2.81 g of the 3-(3-diethylaminopropylamino)-4-chloroindazole, 2.06 g of isopropyl bromide and 20 ml of diethyl ether. Into the solution were introduced dried oxygen gas and dried carbon dioxide gas for 10 hours so as to reflux the solution, and the solution was left to stand for 12 hours. The pH of the solution was adjusted to 4.0 by adding dropwise sulfuric acid to the solution at 0° C. The solution was added with 50 ml of water and filtered. To the aqueous layer of the filtrate was added an aqueous potassium carbonate solution to separate crystals. The crystals were obtained by filtration and dried to give 1.08 g of 3-(3-diethylaminopropylamino)-4-hydroxyindazole having the following analytical values in a yield of 41%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04533731 |
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| Source dataset | uspto-grants-1985_08 |
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| ORD ID | ord-5b8fd00779364e808f7d3d7b6bb29499 |
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| Source note | uspto-grants-1985_08 |
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