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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212025Generated: November 2, 2026

(S)-(4-(3,4-Dichlorobenzyl)morpholin-2-YL)methanamine → n-{[(2s)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-[5-(4-fluorophenyl)-1,2,4oxadiazol-3-yl]acetamide

https://huagongshe.com/reaction/2212025

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(S)-(4-(3,4-Dichlorobenzyl)morpholin-2-YL)methanamineHCID 10171585—
ReactantMethyl (5-(4-fluorophenyl)-1,2,4-oxadiazol-3-yl]acetateHCID 85817174—
CatalystN-methyl-2-pyrrolidoneHCID 13387—
SolventMethanolHCID 887—
Productn-{[(2s)-4-(3,4-Dichlorobenzyl)morpholin-2-yl]methyl}-2-[5-(4-fluorophenyl)-1,2,4oxadiazol-3-yl]acetamideHCID 6888019857.4%

Reaction Steps

A mixture of Intermediate 38 (0.024 g), Intermediate 9 (0.025 g), and 1-methyl-2-pyrrolidinone (1 drop) was subjected was subjected to irradiation in a 600 W microwave oven on full power for 4 mins. The reaction mixture was dissolved in methanol and applied to an ion exchange cartridge (2 g Isolute SCX, pre-conditioned with methanol). Elution with methanol (3 column volumes) followed 10% 0.880 ammonia in methanol (2 column volumes) and evaporation of the first basic fraction in vacuo gave the crude product. Purification by Biotage flash column chromatography on silica gel (8 g cartridge), eluting with 100:8:1 dichloromethane/ethanol/0.880 ammonia, gave the title compound as a white solid (0.025 g). LCMS (System A) Rf 2.85 min Mass Spectrum m/z 479, 481 [MH+]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101882B2
Source datasetuspto-grants-2006_09
ORD IDord-b7237dedf4304fe6a8fdb8ecdd4c9e3c
Source noteuspto-grants-2006_09