Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1262053Generated: November 3, 2026

Morpholine → N-(3-Methoxy-4-nitro-phenyl)-N-methyl-2-morpholin-4-yl-acetamide

https://huagongshe.com/reaction/1262053

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
Reactant1-MethylpiperazineHCID 53167—
Reactant2-Chloro-N-(3-methoxy-4-nitro-phenyl)-N-methyl-acetamideHCID 66711289—
ReactantHCID 66712120HCID 66712120—
ProductN-(3-Methoxy-4-nitro-phenyl)-N-methyl-2-morpholin-4-yl-acetamideHCID 66711708—

Reaction Steps

N-(3-Methoxy-4-nitro-phenyl)-N-methyl-2-morpholin-4-yl-acetamide was prepared in an analogous fashion to N-(3-Methoxy-4-nitro-phenyl)-N-methyl-2-(4-methyl-piperazin-1-yl)-acetamide of Example 471a by treating the in situ generated 2-Chloro-N-(3-methoxy-4-nitro-phenyl)-N-methyl-acetamide with morpholine rather than 1-methyl piperazine. After workup the crude product was pumped under high vacuum to remove majority of morpholine, as some carried along in organic phase after extraction. Small residual amounts were separated after subsequent reduction via trituration with Et2O. (1.19 g, 73%). LC/MS (E/I+) 310.11 (M+H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08471005B2
Source datasetuspto-grants-2013_06
ORD IDord-629466b5dd2d44029e78522caaa9f4c7
Source noteuspto-grants-2013_06