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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1062963Generated: November 1, 2026

Triethylamine → 2-Methoxy-N-(4-methoxy-7-phenyl-benzothiazol-2-yl)-benzamide

https://huagongshe.com/reaction/1062963

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Methoxybenzoyl chlorideHCID 88969—
Reactant2-Amino-4-methoxy-7-phenyl-benzothiazoleHCID 22283026—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventTetrahydrofuranHCID 8028—
Product2-Methoxy-N-(4-methoxy-7-phenyl-benzothiazol-2-yl)-benzamideHCID 22283400—

Reaction Steps

To a solution of 2-amino-4-methoxy-7-phenyl-benzothiazole (200 mg, 0.67 mmol) in THF (10 m) was added DMAP (10 mg, 0.08 mmol), triethylamine (163 □1, 1.17 mmol) and 2-methoxybenzoyl chloride (136 □1, 1 mmol) in THF (2 ml). The mixture was then heated to reflux for 2 h, after cooling, it was partitioned between 1:1 AcOEt/THF (70 ml) and 5% NaHCO3 solution (40 ml). The organic phase was washed with saturated NaCl solution (50 ml), dried with Na2SO4, filtered and the solvent removed under reduced presure. The residue was suspended in ether (10 ml), filtered, washed with ether then dried under vacuum (0.05 mmHg, 60° C.), to afford the title compound was a white solid (260 mg, 85% yield), MS: m/e=390.0 (M+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06963000B2
Source datasetuspto-grants-2005_11
ORD IDord-013ebb5218094eb2ba99d3f10dfdc4e9
Source noteuspto-grants-2005_11