HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1863111Generated: October 31, 2026
Triethylamine → 5-Dimethylamino-6-methoxy-8-[1-methyl-4-phthalimidobutylamino]quinoline
https://huagongshe.com/reaction/1863111
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(4-Bromopentyl)phthalimide | HCID 240534 | — |
| Reactant | 8-Amino-5-dimethylamino-6-methoxyquinoline | HCID 612491 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | 5-Dimethylamino-6-methoxy-8-[1-methyl-4-phthalimidobutylamino]quinoline | HCID 618570 | — |
Reaction Steps
A stirred mixture of 17.2 g (0.033 mole) of 8-amino-5-dimethylamino-6-methoxyquinoline and 9.8 g (0.033 mole) of 4-bromo-1-phthalimidopentane was maintained at 145° while 5 ml of triethylamine was added dropwise. Addition of 9.8 g of 4-bromo-1-phthalimidopentane and 5 ml of triethylamine was repeated three more times, at the same temperature (145°) at 2 hr intervals. The mixture was allowed to cool, diluted with acetone and filtered. The filtrate was concentrated to a brown oil which was diluted with ether, washed with 30% KOH and extracted with chloroform. The extract was passed through a silica column and the eluate was concentrated, dissolved in ether, treated with Darco and slowly evaporated to give yellow crystals which, after washing with petroleum ether (bp 20°-40°) weighed 9.5 g and melted at 103°-105°.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04167638 |
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| Source dataset | uspto-grants-1979_09 |
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| ORD ID | ord-306f25fcc1e64e8e975b98d6bbc7d09b |
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| Source note | uspto-grants-1979_09 |
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