HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 746829Generated: October 25, 2026
1,10-Phenanthroline → 2-{2-methoxy-4-[3-(1,3-thiazol-2-yl)-1H-pyrrol-1-yl]phenyl}pyridine
https://huagongshe.com/reaction/746829
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | 1,4-Dioxane | HCID 31275 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 2-(1H-Pyrrol-3-yl)-1,3-thiazole | HCID 136249894 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Product | 2-{2-methoxy-4-[3-(1,3-thiazol-2-yl)-1H-pyrrol-1-yl]phenyl}pyridine | HCID 11348178 | — |
Reaction Steps
A solution of 2-(1H-pyrrol-3-yl)-1,3-thiazole (0.100 g, 0.67 mmol) 3-(3-iodophenyl)pyridine (0.248 g, 0.8 mmol), copper(I) iodide (0.038 g, 0.2 mmol), 1,10-Phenanthroline (0.360 g, 2 mmol), potassium phosphate (0.440 g, 2.0 mmol) in dioxane (2 mL) was heated to 200° C. for ½ hr under microwave irradiation. The reaction mixture was quenched with H2O (30 mL), then extracted with EtOAc (3×30 mL) and the combined organic extracts washed with brine. The organic phase was dried over Na2SO4 and concentrated in vacuo. The crude purified by liquid chromatography on silica gel using an ISCO single channel system (EtOAc 100%) to give 2-{2-methoxy-4-[3-(1,3-thiazol-2-yl)-1H-pyrrol-1-yl]phenyl}pyridine as a slightly yellow oil. The free base in anhydrous diethyl ether was treated with 1.5 equivalent HCL (1M in Ether) to give HCl salt.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07393959B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-bbd17b4fe72045738cc1bd27b67fe1af |
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| Source note | uspto-grants-2008_07 |
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