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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2236112Generated: October 31, 2026

Phenethyl bromide → Ethyl (2-phenethyl-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetate

https://huagongshe.com/reaction/2236112

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhenethyl bromideHCID 7666—
ReactantDiisopropylethylamineHCID 81531—
ReactantEthyl (1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetate hydrochlorideHCID 71552668—
SolventAcetonitrileHCID 6342—
ProductEthyl (2-phenethyl-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetateHCID 8661434760%

Reaction Steps

Step a): To a stirred solution of Intermediate 1 (50 mg, 0.17 mmol) and DIEA (73 μl, 0.42 mmol) in acetonitrile (1 ml) is added (2-bromo-ethyl)-benzene (26 μl, 0.19 mmol). The reaction mixture is stirred at rt overnight. The solvent is removed under reduced pressure and the crude product is purified by silica gel column chromatography (hexane/EtOAc 3:1, 1% NEt3), affording pure ethyl (2-phenethyl-1,2,3,4-tetrahydro-pyrido[4,3-b]indol-5-yl)-acetate (37 mg) in 60% yield: tR (LC-2) 1.69 min; ESI-MS (pos. ion): m/z 363.26 [M+H]+ (calcd 362.46 for C23H26N2O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07714132B2
Source datasetuspto-grants-2010_05
ORD IDord-d215e2c42d424133862cfafa7d3afb6b
Source noteuspto-grants-2010_05