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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Dichloro-1,3,5-triazine | HCID 17810 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Bromo-1,2,3,4-tetrahydroisoquinoline hydrochloride | HCID 22570216 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 6-Bromo-2-(4-chloro-1,3,5-triazin-2-yl)-1,2,3,4-tetrahydroisoquinoline | HCID 77231348 | 46% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09334269B2 |
|---|
| Source dataset | uspto-grants-2016_05 |
|---|
| ORD ID | ord-897a3673e1c94125895df27b8f3ed6ab |
|---|
| Source note | uspto-grants-2016_05 |
|---|