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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1107116Generated: October 31, 2026

4-Methylmorpholine → HCID 18790164, compound

https://huagongshe.com/reaction/1107116

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-MethylmorpholineHCID 7972—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantBenzyloxyamine hydrochlorideHCID 102312—
Reactant1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
ReactantHCID 18790065HCID 18790065—
SolventDichloromethaneHCID 6344—
ProductHCID 18790164HCID 1879016492%

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of 0.4 g (0.99 mmol) of 3-(4-methoxyphenylsulfonyl)-3-ethyl-7-phenylheptanoic acid in 50 mL of methylene chloride is added 0.47 g (2.96 mmol, 3 eq) of O-benzyl-hydroxylamine hydrochloride, 0.13 g (0.247 mmol) of HOBT, 0.54 mL (4.94 mmol, 5 eq) of n-Methylmorpholine (NMM), and 0.25 g (1.28 mmol, 1.3 eq) of EDCl. After stirring for 18 hours at 25° C. the reaction is partitioned between methylene chloride and 1 N HCl. The organic layer is dried over anhydrous Na2SO4 then concentrated in vacuo. Purification by flash silica gel chromatography afforded 0.463 g (92%) of N-benzyloxy-3-(4-methoxyphenylsulfonyl)-3-ethyl-7-phenylheptanamide in the form of a colorless oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06057369
Source datasetuspto-grants-2000_05
ORD IDord-ae3cf789d46f4f84948f048bf0343ab8
Source noteuspto-grants-2000_05