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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 983441Generated: October 30, 2026

2,4-Dichloro-1,3,5-triazine → 1-(4-Chloro-[1,3,5]triazin-2-yl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline

https://huagongshe.com/reaction/983441

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4-Dichloro-1,3,5-triazineHCID 17810—
ReactantDiisopropylethylamineHCID 81531—
Reactant7-(Trifluoromethyl)-1,2,3,4-tetrahydroquinolineHCID 2781139—
SolventDimethylformamideHCID 6228—
Product1-(4-Chloro-[1,3,5]triazin-2-yl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinolineHCID 22496106—

Reaction Conditions

Temperature0 °C

Reaction Steps

7-(Trifluoromethyl)-1,2,3,4-tetrahydroquinoline (440 mg, 2.2 mmol) was dissolved in DMF (10 mL) under N2 at RT. DIEA (284 mg, 2.2 mmol) was added, and the reaction solution was cooled to 0° C. 2,4-Dichloro-1,3,5-triazine was added, and reaction was stirred with gradual warming to RT. The reaction was quenched after 3 h with water, which caused a fine precipitate to form, which is not filterable. This mixture was extracted 3 times with EtOAc. The EtOAc extracts were washed brine, combined, dried over Na2SO4, filtered, concentrated, and dried under high vacuum giving 1-(4-chloro-[1,3,5]triazin-2-yl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline as a yellow oil that was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06864255B2
Source datasetuspto-grants-2005_03
ORD IDord-efd3550b9fda4398976af6fd145b6557
Source noteuspto-grants-2005_03