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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 522848Generated: October 26, 2026

2,4-Dichloro-1,3,5-triazine → 6-Bromo-2-(4-chloro-1,3,5-triazin-2-yl)-1,2,3,4-tetrahydroisoquinoline

https://huagongshe.com/reaction/522848

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-1,3,5-triazineHCID 17810—
ReactantDiisopropylethylamineHCID 81531—
Reactant6-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochlorideHCID 22570216—
SolventDimethylformamideHCID 6228—
Product6-Bromo-2-(4-chloro-1,3,5-triazin-2-yl)-1,2,3,4-tetrahydroisoquinolineHCID 7723134846%

Reaction Conditions

Temperature0 °C

Reaction Steps

2,4-Dichloro-1,3,5-triazine (2.01 g, 12.7 mmol) was dissolved in 10 mL of dry DMF and the solution was cooled to 0° C. To this solution was added N,N-diisopropylethylamine, (6.65 mL, 38.2 mmol) and 6-bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride (3.26 g, 12.7 mmol). The resulting reaction mixture was stirred at 0° C. to RT for 1.5 h. The reaction mixture was quenched with water (10 mL) and extracted with EtOAc. The organics were dried with MgSO4, filtered and concentrated under reduced pressure. The crude material obtained was purified with medium pressure silica gel chromatography using gradient eluent, 0-40% EtOAc in hexanes to afford 6-bromo-2-(4-chloro-1,3,5-triazin-2-yl)-1,2,3,4-tetrahydroisoquinoline (1.90 g, 46% yield) as white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09334269B2
Source datasetuspto-grants-2016_05
ORD IDord-897a3673e1c94125895df27b8f3ed6ab
Source noteuspto-grants-2016_05