HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082467Generated: October 28, 2026
Sodium Iodide → 7-[3-[[(2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-one
https://huagongshe.com/reaction/2082467
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2H-1-Benzopyran-2-one, 7-(3-chloropropoxy)- | HCID 1900666 | — |
| Reactant | N-Ethyl-2,3-dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine | HCID 19778687 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[3-[[(2,3-Dihydro-7-hydroxy-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-one | HCID 19778664 | 13.5% |
Reaction Steps
N-Ethyl-2,3-dihydro-7-hydroxy-1,4-benzodioxin-2-methanamine (2.11 g, 13.1 mmole), 7-(3-chloropropoxy)coumarin (3.44 g, 14.4 mmole), diisopropylethylamine (11 ml, 63.2 mmole) and sodium iodide (1.98 g, 13.2 mmole) were combined in 175 ml of DMF and heated at 94° C. for 2 days under a nitrogen atmosphere. The solvent was then removed in vacuum and the residue column chromatographed on silica gel using first 0.5% methanol/dichloromethane and then 1.5% methanol/dichloromethane as eluant. The product-containing fractions were combined and concentrated in vacuum and the residue redissolved in dichloromethane and boiled on a hot plate, the dichloromethane gradually being replaced with isopropanol. 4N HCl/isopropanol (4 ml) was added and the title compound was collected by filtration. A second recrystallization from isopropanol yielded 0.73 g of white solid, monohydrochloride, m.p. 208°-215° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05189171 |
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| Source dataset | uspto-grants-1993_02 |
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| ORD ID | ord-0b2d4ea816b947609d6a4297e9ec3c87 |
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| Source note | uspto-grants-1993_02 |
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