HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400627Generated: October 27, 2026
1,10-Phenanthroline → HCID 59455182, compound
https://huagongshe.com/reaction/1400627
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1H-Pyrido[4,3-b]indole, 2,3,4,5-tetrahydro-2,8-dimethyl- | HCID 209291 | — |
| Reactant | 1-(Bromoethynyl)-4-chlorobenzene | HCID 640390 | — |
| Catalyst | Copper Sulfate | HCID 24462 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59455182 | HCID 59455182 | 11.3% |
Reaction Steps
2,8-Dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (200 mg, 1 mmol) was dissolved in toluene (8-10 mL). Copper sulfate (50 mg, 0.2 mmol), 1,10-phenanthroline (72 mg, 0.4 mmol), potassium phosphate (425 mg, 2 mmol) and 1-(bromoethynyl)-4-chlorobenzene (237 mg, 1.1 mmol) was added and the mixture flushed with nitrogen. The reaction mixture was heated at 80° C. overnight (16 h). Product was detected by LCMS. The reaction mixture was filtered through Celite, washed with DCM. The combined organic layer was concentrated under vacuum to obtain product, which was purified by column chromatography (Silica gel-60-80% EtOAc in hexane) to obtain product (38 mg) as a yellow solid. 1H NMR (CDCl3, TFA salt) δ (ppm): 7.52-7.40 (m, 3H), 7.36-7.30(m, 2H), 7.20 (s, 1H), 7.12-7.09 (d, 1H), 3.77 (s, 2H), 3.06-2.94 (m, 4H), 2.62 (s, 3H), 2.42(s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08906925B2 |
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| Source dataset | uspto-grants-2014_12 |
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| ORD ID | ord-91d267a9ae75438bb1f405158dde0254 |
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| Source note | uspto-grants-2014_12 |
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