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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 515162Generated: October 29, 2026

Morpholine → HCID 72187884, compound

https://huagongshe.com/reaction/515162

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantCesium carbonateHCID 10796—
ReactantBinap, (A+-)-HCID 634876—
ReactantHCID 86699733HCID 86699733—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventWaterHCID 962—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 72187884HCID 7218788429%

Reaction Conditions

Temperature40 °C

Reaction Steps

To a stirred solution of 4-bromo-N-[(4-chlorophenyl)-methyl]-2-methoxy-6-methyl-benzamide (0.37 g, 1.02 mmol) in N-methyl-2-pyrrolidone (1 ml) is added morpholine (0.10 ml, 1.20 mmol) at RT. The reaction mixture is degassed and flushed with argon for 30 min followed by addition of caesium carbonate (0.49 g, 1.52 mmol). The reaction mixture is heated to 40° C. At this temperature are added tris(dibenzylideneacetone)dipalladium(0) (0.009 g, 0.01 mmol) and 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (0.019 g, 0.030 mmol) and stirred at 110° C. for 16 h. After completion of the reaction (monitored by TLC), the mixture is diluted with water (20 ml) and extracted with ethyl acetate (3×20 ml). The organic layer is washed with water (20 ml), brine (20 ml), dried over anhydrous sodium sulfate and evaporated to get the crude product, which is purified by column chromatography (silica gel, 20% acetone/hexane) to yield N-[(4-chlorophenyl)-methyl]-2-methoxy-6-methyl-4-morpholin-4-yl-benzamide (example 10) (0.11 g, 0.29 mmol, 29%). [M+H]+ 375.2.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09108936B2
Source datasetuspto-grants-2015_08
ORD IDord-3b5514f2e5494bd6abecad4905a3676d
Source noteuspto-grants-2015_08