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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 427340Generated: October 26, 2026

Triethylamine → N-(4-Morpholinophenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamide

https://huagongshe.com/reaction/427340

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantThionyl ChlorideHCID 24386—
ReactantBenzenamine, 4-(4-morpholinyl)-HCID 75655—
Reactant5-Methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acidHCID 18622509—
SolventWaterHCID 962—
SolventTolueneHCID 1140—
SolventDichloromethaneHCID 6344—
ProductN-(4-Morpholinophenyl)-5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxamideHCID 1862249392.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 5-methoxy-8-nitro-1,2,3,4-tetrahydronaphthalene-2-carboxylic acid (1.3 g, 5 mmol), toluene (20 mL) and thionyl chloride (1.8 mL, 25 mmol) was heated at 80° C. for 1 h. The solvents were removed in vacuo and the residue, dissolved in methylene chloride (10 mL), was added to a solution of 4-morpholinoaniline (890 mg, 5 mmol) and triethylamine (1.0 g, 10 mmol) in methylene chloride (20 mL) at 0° C. The mixture was stirred at 20° C. for 2 h, water was added and the precipitate was filtered to yield 1.9 g (90%) of the title product as crystals: mp 251-253° C.; EIMS (70 eV) m/z (relative intensity) 411 (100, M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06313118B1
Source datasetuspto-grants-2001_11
ORD IDord-23a6db9b2c724219a20e1a02997779ab
Source noteuspto-grants-2001_11