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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218500Generated: October 27, 2026

Phenacyl bromide → N-(3-Morpholinopropyl)-N-(4-phenylthiazol-2-yl)thiophene-2-carboxamide

https://huagongshe.com/reaction/2218500

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenacyl bromideHCID 6259—
Reactant2-Thiophenecarbonyl chlorideHCID 78928—
ReactantDiisopropylethylamineHCID 81531—
ReactantN-[3-(4-Morpholinyl)propyl]thioureaHCID 2760135—
SolventEthanolHCID 702—
ProductN-(3-Morpholinopropyl)-N-(4-phenylthiazol-2-yl)thiophene-2-carboxamideHCID 113951354%

Reaction Steps

A mixture of 2-bromoacetophenone (60 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 (67 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 413.9 [M+H]. HPLC retention time (Method A)=2.78 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07410988B2
Source datasetuspto-grants-2008_08
ORD IDord-9e8693a65c53459cbedd2ea2b738c445
Source noteuspto-grants-2008_08