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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506831Generated: October 31, 2026

Ammonia → 4-[4-((R)-3-Amino-2-hydroxy-propylamino)-phenyl]-morpholin-3-one hydrochloride

https://huagongshe.com/reaction/1506831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantMethaneHCID 297—
Reactant4-[4-(N-(3-chloro-(2R)-2-hydroxy-1-propyl)amino)phenyl]morpholin-3-oneHCID 58137663—
Product4-[4-((R)-3-Amino-2-hydroxy-propylamino)-phenyl]-morpholin-3-one hydrochlorideHCID 7087327375.4%

Reaction Steps

30.00 g of 4-[4-((R)-3-chloro-2-hydroxy-propylamino)-phenyl]-morpholin-3-one (CHP-APMO) (MW=284.75; 1 eq.) were added to 1298 g of conc. aqueous ammonia (MW 17.03; 181 eq.). The reaction mixture was stirred for 2.5 h at room temperature. Then 3.0 g of charcoal were added and after 10 min of stirring, the suspension was filtered and the cake was washed with 90 mL of water. Filtrate and wash water were combined and concentrated in vacuo to a mass of 37 g. To the residue were added 107 mL of ethanol. The resulting suspension was stirred for 1 h at ambient temperature and then cooled to 0° C. After stirring for at least 2 h at this temperature, the product was isolated by filtration and the filter cake was washed with 75 mL of ethanol. After drying in vacuo at 30° C., 23.98 g of the crystalline title compound were isolated. Yield=75.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09221771B2
Source datasetuspto-grants-2015_12
ORD IDord-f1a574217f904a67b59ccdf8597d05c5
Source noteuspto-grants-2015_12