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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218507Generated: November 1, 2026

2-Thiophenecarbonyl chloride → N-(4-(5-Methyl-1-phenyl-1H-pyrazol-4-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide

https://huagongshe.com/reaction/2218507

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
Reactant2-Bromo-1-(5-methyl-1-phenyl-1H-pyrazol-4-yl)ethan-1-oneHCID 2776439—
Solvent1,4-DioxaneHCID 31275—
ProductN-(4-(5-Methyl-1-phenyl-1H-pyrazol-4-yl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamideHCID 6840724665.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-bromo-1-(5-methyl-1-phenyl-1H-pyrazol-4-yl)-1-ethanone (167 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 (193 mg) as an yellow solid as the hydrochloride salt. LC/MS (ESI) m/z 494.3 [M+H]. HPLC retention time (Method B)=2.72 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410988B2
Source datasetuspto-grants-2008_08
ORD IDord-eb796b82005c43e28c54db1e5731e7b1
Source noteuspto-grants-2008_08