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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218502Generated: October 26, 2026

2-Thiophenecarbonyl chloride → N-(4-(5-Chlorothiophen-2-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/2218502

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantDiisopropylethylamineHCID 81531—
Reactant2-(Bromoacetyl)-5-chlorothiopheneHCID 2063634—
ReactantN-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
SolventEthanolHCID 702—
ProductN-(4-(5-Chlorothiophen-2-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamideHCID 6840681644.8%

Reaction Steps

A mixture of 2-bromo-1-(5-chloro-thiophen-2-yl)-ethanone (72 mg, 0.3 mmol) and (3-morpholin-4-yl-propyl)-thiourea (61 mg, 0.3 mmol) in dry ethanol (3 ml) was heated at reflux for 10 min, cooled to room temperature, and concentrated in vacuo. The resulting residue was suspended in dichloromethane (3 mL) followed by the addition of N,N-diisopropylethylamine (105 μL, 0.6 mmol) and thiophene-2-carbonyl chloride (34 μL, 0.32 mmol). The reaction mixture was maintained at room temperature overnight, then concentrated in vacuo. The resulting residue was dissolved in DMSO (1.5 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 (61 mg) as an yellow solid as the hydrochloride salt. LC/MS (ESI) m/z 453.9 [M+H]. HPLC retention time (Method A)=2.93 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410988B2
Source datasetuspto-grants-2008_08
ORD IDord-66ddb412d4fb4039be68a8406bd5ff7b
Source noteuspto-grants-2008_08