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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713971Generated: October 26, 2026

2-Thiophenecarbonyl chloride → N-(4-(2,4-Dimethoxyphenyl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/1713971

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-Bromo-1-(2,4-dimethoxyphenyl)ethanoneHCID 98683—
ReactantN-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-(2,4-Dimethoxyphenyl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamideHCID 6840616772.8%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-bromo-2′,4′-dimethoxyacetophenone (156 mg, 0.6 mmol) and (3-morpholin-4-yl-propyl)-thiourea (122 mg, 0.6 mmol) in dry dioxane (5 ml) was heated at 80° C. for 2 h, cooled to room temperature, and concentrated in vacuo. The resulting residue was suspended in dichloromethane (5 mL) followed by the addition of N,N-diisopropylethylamine (209 μL, 1.2 mmol) and thiophene-2-carbonyl chloride (96 μL, 0.9 mmol). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (2.5 mL) and subjected to HPLC purification (Method Y). The resulting free amine was dissolved in MeOH (1 mL) and 1M HCl/ether (50 mL) was added. The precipitate was filtered and dried in vacuo to provide the title compound (207 mg) as an yellow solid as the hydrochloride salt. LC/MS (ESI) m/z 474.3 [M+H]. HPLC retention time (Method A)=2.81 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795290B2
Source datasetuspto-grants-2010_09
ORD IDord-e6276033429d4d09be7db005aca18d2c
Source noteuspto-grants-2010_09