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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400449Generated: October 31, 2026

Potassium Phosphate, Tribasic → (Z)-5-(2-(2-chlorophenyl)prop-1-enyl)-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/1400449

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantL-ProlineHCID 145742—
Reactant1H-Pyrido[4,3-b]indole, 2,3,4,5-tetrahydro-2,8-dimethyl-HCID 209291—
Reactant1-(1-Bromoprop-1-en-2-yl)-2-chlorobenzeneHCID 86642477—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product(Z)-5-(2-(2-chlorophenyl)prop-1-enyl)-2,8-dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 59454945—

Reaction Steps

2,8-Dimethyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (200 mg, 1 mmol) was dissolved in DMF. Copper (I) iodide (19 mg, 0.1 mmol), L-proline (23 mg, 0.2 mmol) and potassium phosphate (424 mg, 2 mmol) were added and the reaction mixture was stirred for 10 min. at RT. 1-(1-Bromoprop-1-en-2-yl)-2-chlorobenzene (277 mg, 1.2 mmol) was added dropwise and the reaction mixture was purged with nitrogen. The reaction mixture was heated overnight at 85° 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 0-5% MeOH-DCM. Yield: 0.37 mg as the TFA salt. 1H NMR (CDCl3, TFA salt) δ (ppm): 7.25 (m, 2H), 7.10 (t, 1H), 7.05 (s, 1H), 7.0 (m, 2H), 6.90 (d, 1H), 6.75 (s, 1H), 4.40 (d, 1H), 4.0 (d, 1H), 3.40 (m, 1H), 3.20 (m, 1H), 2.90 (m, 1H), 2.80 (s, 3H), 2.65 (m, 1H), 2.40 (s, 3H), 2.30 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906925B2
Source datasetuspto-grants-2014_12
ORD IDord-2a12b4d238ee44269a022ed8792bb673
Source noteuspto-grants-2014_12