HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 581795Generated: October 30, 2026
Ethylamine hydrochloride → HCID 70180694, compound
https://huagongshe.com/reaction/581795
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethylamine hydrochloride | HCID 11198 | — |
| Reactant | 1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide | HCID 15908 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | HCID 54355870 | HCID 54355870 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 70180694 | HCID 70180694 | 86.9% |
Reaction Steps
To a mixture of 8-[3-[N-(4-carboxycinnamoylglycyl)-N-methylamino]-2,6-dichlorobenzyloxy]-2-methylquinoline (100 mg), ethylamine hydrochloride (16.9 mg) and N,N-dimethylformamide (2 ml) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide (32.2 mg) and 1-hydroxybenzotriazole (30.4 mg), and the mixture was stirred for 6 hours at ambient temperature. The mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water, saturated sodium bicarbonate solution and brine, dried over magnesium sulfate, and concentrated in vacuo. The residue was purified by preparative thin-layer chromatography (methylene chloride--methanol) to give 8-[2,6-dichloro-3-[N-[4-(ethylcarbamoyl)cinnamoylglycyl]-N-methylamino]benzyloxy]-2-methylquinoline (91 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05922711 |
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| Source dataset | uspto-grants-1999_07 |
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| ORD ID | ord-19bb243c290a46fd9d0e348e9dc5fa90 |
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| Source note | uspto-grants-1999_07 |
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