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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2194000Generated: October 26, 2026

Morpholine-4-sulfonyl chloride → 4-(2-Methoxy-ethyl)-1-(morpholine-4-sulfonyl)-piperidine-4-carboxylic acid ethyl ester

https://huagongshe.com/reaction/2194000

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholine-4-sulfonyl chlorideHCID 12798265—
Reactant4-(2-Methoxy-ethyl)-piperidine-4-carboxylic acid ethyl esterHCID 56753969—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
Product4-(2-Methoxy-ethyl)-1-(morpholine-4-sulfonyl)-piperidine-4-carboxylic acid ethyl esterHCID 66787287—

Reaction Conditions

Temperature0 °C

Reaction Steps

4-(2-Methoxy-ethyl)-piperidine-4-carboxylic acid ethyl ester (0.646 g) dissolved in methylene chloride (10 ml) under an argon atmosphere were treated with DMAP (0.673 g) at RT, the mixture was cooled to 0° C. and morpholine-4-sulfonylchloride (0613 g) in methylene chloride (2 ml) was added dropwise. The mixture was stirred for 12 h at RT then partitioned between methylen chloride and 1 M HCl. The layers were separated, the organic layer washed with 2M aqueous KHCO3 then dried over Na2SO4. The solvent was evaporated off, the residue purified by flash chromatography (AcOEt/heptane, gradient from 0 to 50%) to give 4-(2-methoxy-ethyl)-1-(morpholine-4-sulfonyl)-piperidine-4-carboxylic acid ethyl ester, (0.68 g) as a light yellow solid. MS (ESI): 365.17 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08329904B2
Source datasetuspto-grants-2012_12
ORD IDord-a8643b2fcc044fa8b1b14167b2cbc5f4
Source noteuspto-grants-2012_12