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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1401558Generated: October 30, 2026

8-chloro-2-methyl-1H,2H,3H,4H,5H-pyrido(4,3-b)indole → HCID 59455076, compound

https://huagongshe.com/reaction/1401558

Reaction equation

Participants

RoleNameHCIDCharge
Reactant8-chloro-2-methyl-1H,2H,3H,4H,5H-pyrido(4,3-b)indoleHCID 19615—
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantL-ProlineHCID 145742—
Reactant1-(2-Bromo-1-methylethenyl)-2,4-difluorobenzeneHCID 73083491—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethylformamideHCID 6228—
ProductHCID 59455076HCID 59455076—

Reaction Steps

8-Chloro-2-methyl-2,3,4,5-tetrahydro-1H-pyrido[4,3-b]indole (220 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-(2-Bromo-1-methyl-vinyl)-2,4-difluoro-benzene (279 mg, 1.2 mmol) was added dropwise and the reaction mixture was purged with nitrogen. The reaction mixture was heated 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 0-2% MeOH-DCM. The product was further purified by HPLC. Yield: 12 mg. 1H NMR (CD3OD, freebase) δ (ppm): 7.58 (m, 2H), 7.40 (s, 1H), 7.14 (s, 1H), 7.12 (d, 1H), 7.05 (m, 2H), 3.70 (s, 2H), 2.95 (m, 2H), 2.85 (m, 2H), 2.40 (s, 3H), 1.82 (s, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08907097B2
Source datasetuspto-grants-2014_12
ORD IDord-0875d73a72284e8480ab8bd158e95ae5
Source noteuspto-grants-2014_12