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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400627Generated: October 27, 2026

1,10-Phenanthroline → HCID 59455182, compound

https://huagongshe.com/reaction/1400627

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,10-PhenanthrolineHCID 1318—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant1H-Pyrido[4,3-b]indole, 2,3,4,5-tetrahydro-2,8-dimethyl-HCID 209291—
Reactant1-(Bromoethynyl)-4-chlorobenzeneHCID 640390—
CatalystCopper SulfateHCID 24462—
SolventTolueneHCID 1140—
ProductHCID 59455182HCID 5945518211.3%

Reaction Conditions

Temperature80 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906925B2
Source datasetuspto-grants-2014_12
ORD IDord-91d267a9ae75438bb1f405158dde0254
Source noteuspto-grants-2014_12