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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1158124Generated: October 27, 2026

1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → 2-(4-Fluoro-3-methyl-benzyl)-hexanoic acid (tetrahydro-pyran-2-yloxy)-amide

https://huagongshe.com/reaction/1158124

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantN-MethylmorphineHCID 61063—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantO-(Tetrahydropyran-2-yl)hydroxylamineHCID 5142091—
Reactant2-(4-Fluoro-3-methyl-benzyl)-hexanoic acidHCID 59512599—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-(4-Fluoro-3-methyl-benzyl)-hexanoic acid (tetrahydro-pyran-2-yloxy)-amideHCID 5951259560%

Reaction Steps

To a solution of 2-(4-Fluoro-3-methyl-benzyl)-hexanoic acid (0.498 g, 2.091 mmol), O-(tetrahydro-pyran-2-yl)-hydroxylamine (0.735 g, 6.274 mmol), HOBT (0.282 g, 2.091 mmol), and N-methyl morphine (1.058 g, 10.455 mmol) in 20 mL of dichloromethane, was added EDCI (0.601 g, 3.137 mmol). After stirring at room temperature under N2 for 64 h, the reaction mixture was diluted with 60 mL of water and extracted with dichloromethane (60 mL×3). The organic extracts were combined and dried over anhydrous Na2SO4. After removing the solvents under reduced pressure, the product was isolated by Flash chromatography (silica gel) eluting with 0-40% ethyl acetate/hexanes to give the title compound as a pale yellow solid (0.423 g, 60% yield). LC-MS: tR=9.1 min; m/z 338 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807720B2
Source datasetuspto-grants-2010_10
ORD IDord-5a64fc5584e641d3af056664a5ca161b
Source noteuspto-grants-2010_10