HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2082475Generated: October 27, 2026
N-Ethyl-2,3-dihydro-1,4-benzodioxin-2-methanamine → 7-[3-[[(2,3-Dihydro-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-one
https://huagongshe.com/reaction/2082475
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | N-Ethyl-2,3-dihydro-1,4-benzodioxin-2-methanamine | HCID 30614 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-(3-bromopropoxy)-2H-chromen-2-one | HCID 2757176 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 7-[3-[[(2,3-Dihydro-1,4-benzodioxin-2-yl)methyl]ethylamino]propoxy]-2H-1-benzopyran-2-one | HCID 19778684 | 51.6% |
Reaction Steps
N-Ethyl-2,3-dihydro-1,4-benzodioxin-2-methanamine (4.67 g, 24.2 mmole), 7-(3-bromopropoxy)coumarin (6.92 g, 24.4 mmole), and diisopropylethylamine (6.70 ml, 38.5 mmole) were combined in 300 ml of DMF and heated at 76° C. for 24 hours under a nitrogen atmosphere. The solvent was then removed in vacuum and replaced with dichloromethane. The mixture was washed with an equal volume of saturated aqueous sodium bicarbonate, dried over magnesium sulfate, filtered and concentrated in vacuum. The residue (10 g) was column chromatographed on 225 g of silica gel using 40% ethyl acetate/dichloromethane as eluant. The product-containing fractions were concentrated in vacuum and the residue crystallized from isopropanol with the addition of 30 ml of 4N isopropanolic HCl to give 4.94 g of the title compound as a white solid, monohydrochloride, m.p. 147°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05189171 |
|---|
| Source dataset | uspto-grants-1993_02 |
|---|
| ORD ID | ord-7155d65dfa884794ae690469367ca06c |
|---|
| Source note | uspto-grants-1993_02 |
|---|