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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2084522Generated: October 31, 2026

4-Methylmorpholine → HCID 59909776, compound

https://huagongshe.com/reaction/2084522

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
ReactantO-BenzylhydroxylamineHCID 102313—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
Reactant1-Hydroxybenzotriazole hydrateHCID 2796029—
ReactantHCID 59909762HCID 59909762—
ProductHCID 59909776HCID 5990977698.9%

Reaction Steps

A solution of (3R)-6-cyclohexyl-3-[4-(methoxycarbonyl)-5-methyl-1,3-oxazol-2-yl]hexanoic acid (Preparation 174) (2.48 g, 7.36 mmol) was cooled to 0° and treated with 1-hydroxybenzotriazole hydrate (994 mg, 7.36 mmol), 1-[3-(dimethylamino)propyl]-3-ethylcarbodiimide hydrochloride (2.12 g, 11.06 mmol) and N-methylmorpholine (1.21 ml, 11.04 mmol). The mixture was stirred for 15 minutes then treated with O-benzylhydroxyamine (1.17 g, 7.36 mmol) and further N-methylmorpholine (0.81 ml, 7.36 mmol). The mixture was stirred for 1 hour being allowed to warm to room temperature over this time. The solvent was removed under reduced pressure and the residue was dissolved in ethyl acetate, washed sequentially with water, a saturated solution of sodium hydrogen carbonate and brine, dried over anhydrous magnesium sulphate, filtered and the solvent removed under reduced pressure to afford the title compound as a colourless oil (3.22 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06716861B2
Source datasetuspto-grants-2004_04
ORD IDord-1e59a4f2688b40978f6f4556dadbd0b8
Source noteuspto-grants-2004_04