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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phenacyl bromide | HCID 6259 | — |
| Reactant | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | N-[3-(4-Morpholinyl)propyl]thiourea | HCID 2760135 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(3-Morpholinopropyl)-N-(4-phenylthiazol-2-yl)thiophene-2-carboxamide | HCID 1139513 | 54% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07410988B2 |
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| Source dataset | uspto-grants-2008_08 |
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| ORD ID | ord-9e8693a65c53459cbedd2ea2b738c445 |
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| Source note | uspto-grants-2008_08 |
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