HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1045628Generated: October 27, 2026
1,10-Phenanthroline → HCID 59368234, compound
https://huagongshe.com/reaction/1045628
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 1-(Bromoethynyl)-4-chlorobenzene | HCID 640390 | — |
| Reactant | 9-Chloro-3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole | HCID 68558507 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 59368234 | HCID 59368234 | 10% |
Reaction Steps
A mixture of 9-chloro-3-methyl-1,2,3,4,5,6-hexahydroazepino[4,5-b]indole (235 mg, 1 mmol), CuSO4.5H2O (50 mg, 0.2 mmol), 1,10-Phenanthroline (72 mg, 0.4 mmol), K3PO4 (425 mg, 2 mmol) and 1-(bromoethynyl)-4-chlorobenzene (237 mg, 1.1 mmol) in toluene (10 mL) was flushed with nitrogen heated 80° C. for 16 h. The reaction was monitored by LCMS. The reaction mixture was filtered through Celite, washed with DCM. The organic layer was concentrated and purified by column chromatography (silica gel, 60-80% ethyl acetate in hexane) to get 37 mg of product. 1H NMR (CDCl3, HCl salt) δ (ppm): 7.50 (s, 1H) 7.49-7.40 (m, 3H), 7.38-7.32(m, 2H), 7.25-7.20 (d, 1H), 3.22-3.18 (m, 2H), 3.0-2.90 (m, 6H), 2.60 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08569287B2 |
|---|
| Source dataset | uspto-grants-2013_10 |
|---|
| ORD ID | ord-01722434d0cc499cb290a0312c76070f |
|---|
| Source note | uspto-grants-2013_10 |
|---|