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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1111731Generated: October 25, 2026

Hydrochloric Acid → N-methyl-3-morpholino-2-(2-pyridyl)thiopropanamide

https://huagongshe.com/reaction/1111731

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethyl isothiocyanateHCID 11167—
Reactant4-(2-(2-Pyridyl)ethyl)morpholineHCID 95909—
ReactantHCID 178506676HCID 178506676—
SolventBenzeneHCID 241—
SolventWaterHCID 962—
SolventBenzene etherHCID 22174802—
ProductN-methyl-3-morpholino-2-(2-pyridyl)thiopropanamideHCID 15581964—

Reaction Steps

N-[2-(2-pyridyl)ethyl]morpholine (12.7 g., 0.07 mole) in 60 ml. of dry benzene is added dropwise to 35 ml. of 2M phenyl lithium (0.07 mole) in benzene/ether with cooling. The mixture is stirred for 30 minutes, then methyl isothiocyanate (5.2 g., 0.07 mole), dissolved in 60 ml. of dry benzene, is added dropwise with cooling. The resulting solution is stirred overnight. An equal volume of water is added and the solution is cooled and made acidic with 10% hydrochloric acid. The phases are separated, the organic phase is washed with water, and the combined aqueous phases are made basic to about pH 9, then extracted with chloroform. The chloroform extracts are washed with water and dried over magnesium sulfate. Filtration and removal of solvent gives a residue which is recrystallized from ethyl acetate to give N-methyl-3-morpholino-2-(2-pyridyl)thiopropanamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04118567
Source datasetuspto-grants-1978_10
ORD IDord-bbfc17e6d5a8488c80a34cbd44f80e2f
Source noteuspto-grants-1978_10