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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 538296Generated: October 29, 2026

Phosphorus sulfide (P2S5) → 5-(6-Bromo-pyridin-2-yl)-5-methyl-morpholine-3-thione

https://huagongshe.com/reaction/538296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus sulfide (P2S5)HCID 14817—
Reactant5-(6-Bromo-pyridin-2-yl)-5-methyl-morpholin-3-oneHCID 86668011—
SolventHydrochloric AcidHCID 313—
SolventPyridineHCID 1049—
SolventEthyl AcetateHCID 8857—
Product5-(6-Bromo-pyridin-2-yl)-5-methyl-morpholine-3-thioneHCID 86668013—

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-(6-bromo-pyridin-2-yl)-5-methyl-morpholin-3-one (4.65 g, 17.15 mmol) and P2S5 (4.57 g, 20.58 mmol) in pyridine (60 ml) was stirred at 80° C. under N2 for 6 h. The reaction mixture was cooled to rt and diluted with 0.5N aq. HCl and EtOAc. The phases were separated and the aq. phase was twice extracted with EtOAc. The combined org. phases were washed with brine, dried over Na2SO4, filtered and concentrated. The title compound was obtained as a pale yellow solid after flash chromatography on silica gel (cyclohexane/EtOAc 100:0 to 75:25). HPLC RtH4=0.89 min; ESIMS: 287, 289 [(M+H)+]; 1H NMR (400 MHz, DMSO-d6): δ 11.15 (s, 1H), 7.86-7.82 (m, 1H), 7.61 (dd, 1H), 7.39 (dd, 1H), 4.44-4.34 (d, 2H), 4.13 (d, 1H), 3.74 (d, 1H), 1.52 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08865712B2
Source datasetuspto-grants-2014_10
ORD IDord-324315e69ecb46b79859763a45f6663e
Source noteuspto-grants-2014_10