HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108648Generated: October 31, 2026
HCID 18783946, compound → HCID 18783941, compound
https://huagongshe.com/reaction/1108648
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18783946 | HCID 18783946 | — |
| Catalyst | HCID 178418390 | HCID 178418390 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 18783941 | HCID 18783941 | 75.4% |
Reaction Steps
2.50 g (6.33 mmol) of 4-[4-(tert-Butoxycarbonylamino)butylamino]-2-chloro-3-nitroquinoline was dissolved in 65 ml of methanol and 1 g of 10% palladium-carbon was added thereto. The mixture was stirred for one day under hydrogen atomosphere. The reaction mixture was filtered, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform:methanol=10:1 (v/v)). Finally, the resulting product was triturated with diethyl ether and collected by filtration to obtain 1.75 g (4.77 mmol) of 3-amino-4-[4-(tert-butoxycarbonylamino)butylamino]quinoline hydrochloride shown below as a yellow solid. ##STR57## Its spectroscopic data are as follows: IR (KBr) cm-1 : 3340, 2970, 1690, 1590, 1530, 1170.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06069149 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-82244d514bbf4a1bb2e4af4cd130412c |
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| Source note | uspto-grants-2000_05 |
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