HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 393265Generated: October 30, 2026
4-Pyridineethanamine → HCID 9953325, compound
https://huagongshe.com/reaction/393265
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 4-Pyridineethanamine | HCID 83275 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 1-Hydroxybenzotriazole hydrate | HCID 2796029 | — |
| Reactant | 7-Methoxy-2-oxo-8-pentyloxy-1,2-dihydroquinoline-3-carboxylic acid | HCID 9904595 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 9953325 | HCID 9953325 | 87% |
Reaction Steps
7-Methoxy-2-oxo-8-pentyloxy-1,2-dihydroquinoline-3-carboxylic acid (30.0 mg) obtained in Example 2-1, 2-pyridine-4-ylethylamine (36.0 mg), and 1-hydroxybenzotriazole hydrate (17.3 mg) were dissolved in dimethylformamide (2 ml), and 1-ethyl-3-(3-dimethyl-aminopropyl)carbodiimide hydrochloride (24.5 mg) was successively added to this solution while being cooled with ice. After the reaction solution was stirred at room temperature for 5 hours, ethyl acetate (3 ml) and a saturated aqueous solution of sodium hydrogencarbonate (3 ml) were added to this solution. The organic layer was separated and dried over anhydrous sodium sulfate, filtered to remove the desiccating agent, and concentrated under reduced pressure. The resultant residue was purified through column chromatography (eluent: a mixture of chloroform and methanol at a ratio of 25:1) to obtain the title compound (35 mg) as colorless crystals (Table 8).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06806276B2 |
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| Source dataset | uspto-grants-2004_10 |
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| ORD ID | ord-d580c6657fa94e0db33e7441fa625a6a |
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| Source note | uspto-grants-2004_10 |
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