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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1400438Generated: November 1, 2026

Potassium Phosphate, Tribasic → (E)-8,9-dichloro-5-(2-(4-fluorophenyl)prop-1-enyl)-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole

https://huagongshe.com/reaction/1400438

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantL-ProlineHCID 145742—
Reactant8,9-Dichloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 67312484—
Reactant(1-Bromoprop-1-en-2-yl)-4-fluorobenzeneHCID 86644757—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
Product(E)-8,9-dichloro-5-(2-(4-fluorophenyl)prop-1-enyl)-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indoleHCID 59455167—

Reaction Steps

8,9-Dichloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (200 mg, 0.78 mmol) was dissolved in DMF. Copper (I) iodide (14 mg, 0.078 mmol), L-proline (17 mg, 0.156 mmol) and potassium phosphate (330 mg, 1.56 mmol) were added and the reaction mixture was stirred for 10 min. at RT. 1-(1-Bromoprop-1-en-2-yl)-4-fluorobenzene (200 mg, 0.94 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. The product was further purified by HPLC. 1H NMR (CDCl3, TFA salt) δ (ppm): 7.50 (m, 2H), 7.25 (m, 1H), 7.10 (t, 2H), 7.05 (d, 1H), 6.75 (s, 1H), 5.10 (d, 1H), 4.40 (d, 1H), 3.90 (m, 1H), 3.38 (m, 1H), 3.22 (m, 1H), 3.05 (s, 3H), 2.90 (m, 1H), 1.90 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08906925B2
Source datasetuspto-grants-2014_12
ORD IDord-eb0970647c124e3fb6a5021fd9a586d9
Source noteuspto-grants-2014_12