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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401540Generated: October 31, 2026

Potassium Phosphate, Tribasic → (E)-5-(2-(4-fluorophenyl)prop-1-enyl)-2,3,8-trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/1401540

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantL-ProlineHCID 145742—
Reactant1-(-2-Bromovinyl)-4-fluorobenzeneHCID 53855149—
Reactant2,3,8-Trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 66612087—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product(E)-5-(2-(4-fluorophenyl)prop-1-enyl)-2,3,8-trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 59454983—

Reaction Steps

2,3,8-Trimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (107 mg, 0.5 mmol) was dissolved in DMF. Copper (I) iodide (9.5 mg, 0.05 mmol), L-proline (11.5 mg, 0.1 mmol) and potassium phosphate (414 mg, 2 mmol) were added and the reaction mixture was stirred for 10 min. at RT. 1-(2-bromovinyl)-4-fluorobenzene (107.83 mg, 0.55 mmol) was added dropwise and the reaction mixture was purged with nitrogen. The reaction mixture was heated overnight at 100° C. (prolonged heating in some cases was required). DMF was evaporated under reduced pressure, the residue was diluted with water and the solid was filtered. The solid material was purified by silica gel chromatography (100-200 mesh) eluting with 0-7% MeOH-DCM. Yield: 92 mg. 1H NMR (CD3OD, oxalate salt) δ (ppm): 7.70 (m, 2H), 7.30 (s, 1H), 7.10 (m, 4H), 6.95 (s, 1H), 4.70 (m, 1H), 4.60 (m, 1H), 3.90 (m, 1H), 3.20 (m, 1H), 2.95 (m, 4H), 2.42 (s, 3H), 1.90 (s, 3H), 1.50 (d, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907097B2
Source datasetuspto-grants-2014_12
ORD IDord-5a014c17ff45438d802f5600ca1c8c99
Source noteuspto-grants-2014_12