HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2218506Generated: October 25, 2026
2-Thiophenecarbonyl chloride → N-(3-Morpholinopropyl)-N-(4-(3-phenylisoxazol-5-yl)thiazol-2-yl)thiophene-2-carboxamide
https://huagongshe.com/reaction/2218506
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Thiophenecarbonyl chloride | HCID 78928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 5-(Bromoacetyl)-3-phenylisoxazole | HCID 2735532 | — |
| Reactant | N-[3-(4-Morpholinyl)propyl]thiourea | HCID 2760135 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-(3-Morpholinopropyl)-N-(4-(3-phenylisoxazol-5-yl)thiazol-2-yl)thiophene-2-carboxamide | HCID 59769689 | 53.8% |
Reaction Steps
A mixture of 2-bromo-1-(3-phenylisoxazol-5-yl)ethan-1-one (160 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 (155 mg) as an off-white solid as the hydrochloride salt. LC/MS (ESI) m/z 481.1 [M+H]. HPLC retention time (Method B)=2.94 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-f070a6b203a24f7ba8950c9258e092c2 |
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| Source note | uspto-grants-2008_08 |
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