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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1404792Generated: October 27, 2026

Bis(2-Methoxyethyl)amine → HCID 66994633, compound

https://huagongshe.com/reaction/1404792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBis(2-Methoxyethyl)amineHCID 2383—
ReactantDiethylamineHCID 8021—
Reactant1-HydroxybenzotriazoleHCID 75771—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 54670137HCID 54670137—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 66994633HCID 6699463319.1%

Reaction Steps

To a solution of example 8 (0.150 g, 0.393 mmol) in DMF (1 ml), HOBT (0.063 g, 0.471 mmol), EDC-HCl (0.187 g, 0.983 mmol) and diethyl amine (0.16 ml, 1.17 mmol) were added and stirred for 5 min, Bis(2-methoxyethyl)amine (0.104 g, 0.786 mmol) was added at RT and the reaction mixture was stirred for 12 h. To the reaction mixture water was added and extracted with ethyl acetate, dried over sodium sulphate and concentrated under reduced pressure. The crude product was purified by column chromatography with methanol:dichloromethane to afford the amide as a yellow solid (0.04 g). The amide was dissolved in THF (2 ml), ether saturated with HCl (2 ml) was added at 0° C. and stirred for 15 min. The precipitate formed was washed with ether and dried under vacuum to afford the title compound as a yellow solid (0.035 g, 17%). M.P.: 126-129° C. 1H-NMR (δ ppm, DMSO-d6, 400 MHz): 9.07 (m, 1H), 8.74 (m, 1H), 8.70 (d, J=8.7 Hz, 1H), 8.29 (d, J=8.3 Hz, 2H), 8.19 (m, 3H), 8.02 (m, 1H), 7.78 (m, 1H), 7.53 (d, J=8.2 Hz, 2H), 6.27 (s, 2H), 3.64 (bs, 2H), 3.58 (br.s, 2H), 3.41 (br.s, 4H), 3.30 (s, 3H), 3.16 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912331B2
Source datasetuspto-grants-2014_12
ORD IDord-27dae954e40148759614bc8ed7eb5736
Source noteuspto-grants-2014_12