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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713974Generated: November 3, 2026

2-Thiophenecarbonyl chloride → HCID 68407058, compound

https://huagongshe.com/reaction/1713974

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
Reactant2-Bromo-1-(5-pyridin-2-yl-thiophen-2-yl)-ethanoneHCID 2776201—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 68407058HCID 68407058107.4%

Reaction Conditions

Temperature80 °C

Reaction Steps

A mixture of 2-bromo-1-[5-(2-pyridinyl)-2-thienyl]-1-ethanone (169 mg, 0.6 mmol) (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 (320 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 497.5 [M+H]. HPLC retention time (Method B)=2.55 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07795290B2
Source datasetuspto-grants-2010_09
ORD IDord-b8fdae455a7f4296b83f011f4d9f1e34
Source noteuspto-grants-2010_09