HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1713971Generated: October 26, 2026
2-Thiophenecarbonyl chloride → N-(4-(2,4-Dimethoxyphenyl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide
https://huagongshe.com/reaction/1713971
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 2-Bromo-1-(2,4-dimethoxyphenyl)ethanone | HCID 98683 | — |
| Reactant | N-[3-(4-Morpholinyl)propyl]thiourea | HCID 2760135 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(4-(2,4-Dimethoxyphenyl)thiazol-2-yl)-N-(3-morpholinopropyl)thiophene-2-carboxamide | HCID 68406167 | 72.8% |
Reaction Steps
A mixture of 2-bromo-2′,4′-dimethoxyacetophenone (156 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 (207 mg) as an yellow solid as the hydrochloride salt. LC/MS (ESI) m/z 474.3 [M+H]. HPLC retention time (Method A)=2.81 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07795290B2 |
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| Source dataset | uspto-grants-2010_09 |
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| ORD ID | ord-e6276033429d4d09be7db005aca18d2c |
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| Source note | uspto-grants-2010_09 |
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