HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2198359Generated: October 30, 2026
1,10-Phenanthroline → HCID 57930454, compound
https://huagongshe.com/reaction/2198359
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 1,10-Phenanthroline | HCID 1318 | — |
| Reactant | Potassium Phosphate, Tribasic | HCID 62657 | — |
| Reactant | 6-chloro-2-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole | HCID 15508373 | — |
| Reactant | HCID 59455074 | HCID 59455074 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 57930454 | HCID 57930454 | 18.1% |
Reaction Steps
6-chloro-2-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole (100 mg, 0.45 mmol) was mixed with CuSO4.5H2O (23 mg, 0.090 mmol), 1,10-phenanthroline (33 mg, 0.18 mmol), K3PO4 (192 mg, 0.90 mmol) and 4-(bromoethynyl)-2-fluoro-1-methoxybenzene (113 mg, 0.49 mmol) in toluene (5 ml). The reaction mixture was purged with nitrogen and heated at 80° C. for 16 h. Product was detected by LCMS. The reaction mixture was filtered through Celite and Celite bed was rinsed with dichloromethane. Combined organic layer was concentrated under reduced pressure and the residue was purified by silica gel chromatography (100-200 mesh) eluting with 60-80% ethyl acetate in hexane to obtain 6-chloro-9-((3-fluoro-4-methoxyphenyl)ethynyl)-2-methyl-2,3,4,9-tetrahydro-1H-pyrido[3,4-b]indole (30 mg). 1H NMR (CDCl3) FREE BASE 7.42 (d, 2H), 7.25 (m, 3H), 6.95 (t, 1H), 3.90 (s, 3H), 3.70 (s, 2H), 2.80 (m, 4H), 2.56 (s, 3H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08338447B2 |
|---|
| Source dataset | uspto-grants-2012_12 |
|---|
| ORD ID | ord-bdce72d314ca466881fa94ff64693fa8 |
|---|
| Source note | uspto-grants-2012_12 |
|---|