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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1014019Generated: October 31, 2026

Morpholine → HCID 66878651, compound

https://huagongshe.com/reaction/1014019

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantTriethylamineHCID 8471—
ReactantHCID 86650830HCID 86650830—
SolventMethanolHCID 887—
SolventTetrahydrofuranHCID 8028—
ProductHCID 66878651HCID 66878651—

Reaction Steps

(Step 1) To a solution of morpholine (0.36 ml) and triethylamine (0.58 ml) in methanol (15 ml) was added dropwise a suspension of 2-[(acetylamino)methyl]-4-fluorobenzenesulfonyl chloride (1.00 g) in tetrahydrofuran (5 ml) under ice-cooling, and the mixture was allowed to warm to room temperature, and stirred for 1 hr. The reaction mixture was quenched with saturated brine, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over magnesium sulfate. The solvent was evaporated under reduced pressure. The residue was purified by silica gel chromatography (ethyl acetate). The obtained oil was dissolved in ethanol (20 ml), hydrochloric acid (10 ml) was added, and the mixture was stirred with heating under reflux for 9 hr. The solvent was evaporated under reduced pressure, and the residue was collected by filtration, and washed with ethyl acetate to give 1-[5-fluoro-2-(morpholin-4-ylsulfonyl)phenyl]methanamine hydrochloride (0.58 g) as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07982044B2
Source datasetuspto-grants-2011_07
ORD IDord-46e0a42f1dd045bca83c60e7d49a1aec
Source noteuspto-grants-2011_07