HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1507439Generated: October 29, 2026
Diisopropylethylamine → HCID 71668098, compound
https://huagongshe.com/reaction/1507439
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride | HCID 2723939 | — |
| Reactant | 3,3,3-Trifluoropropionic acid | HCID 2777972 | — |
| Reactant | HCID 117701633 | HCID 117701633 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 71668098 | HCID 71668098 | 13.6% |
Reaction Steps
A solution of 7-hydroxy-3,8-dimethyl-2-(piperidin-4-yl)-4H-chromen-4-one (68 mg, 0.25 mmol) obtained in Example 7-2, 3,3,3-trifluoropropionic acid (33 μL, 0.30 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (192 mg, 1.00 mmol), and diisopropylethylamine (86 μL, 0.50 mmol) in dimethylformamide (1.5 mL) was stirred at room temperature for 4 hours. The reaction solution was concentrated, and water was added to the obtained residue, followed by extraction with ethyl acetate. The organic layer was dried over sodium sulfate. The desiccant was filtered off, and then the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol=100/0→95/5) to obtain 13 mg of the title compound (yield: 13%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09221811B2 |
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| Source dataset | uspto-grants-2015_12 |
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| ORD ID | ord-18e863f3e50940b9a9caaff2a01e4fe0 |
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| Source note | uspto-grants-2015_12 |
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