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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910278Generated: November 3, 2026

Aniline → 2-morpholin-4-ylmethyl-6-nitro-N-phenyl-benzamide

https://huagongshe.com/reaction/1910278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAnilineHCID 6115—
ReactantThionyl ChlorideHCID 24386—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Morpholin-4-ylmethyl-6-nitro-benzoic acidHCID 59841069—
SolventTetrahydrofuranHCID 8028—
Product2-morpholin-4-ylmethyl-6-nitro-N-phenyl-benzamideHCID 59841084—

Reaction Steps

A solution of compound 6 (0.62 g, 2.3 mmol) in THF (50 mL) was treated with thionyl chloride (0.94 mL), stirred at room temperature for 4 h, and evaporated to dryness. The residue was dissolved in THF (50 mL) and treated with aniline (0.58 mL, 6.4 mmol) and diisopropylethylamine (1.12 mL, 6.4 mmol). The reaction mixture was stirred for 4 h, concentrated, dissolved in dichloromethane (50 mL), washed with saturated aqueous sodium bicarbonate (25 mL) and brine (25 mL), dried with sodium sulfate, and concentrated. The crude residue of compound 7 then was purified by flash chromatography (5% methanol in dichloromethane).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE044638E1
Source datasetuspto-grants-2013_12
ORD IDord-b552276f424746eb8d3d59b6f3569582
Source noteuspto-grants-2013_12