HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,4-Dichloro-1,3,5-triazine → 1-(4-Chloro-[1,3,5]triazin-2-yl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,4-Dichloro-1,3,5-triazine | HCID 17810 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 7-(Trifluoromethyl)-1,2,3,4-tetrahydroquinoline | HCID 2781139 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-(4-Chloro-[1,3,5]triazin-2-yl)-7-trifluoromethyl-1,2,3,4-tetrahydro-quinoline | HCID 22496106 | — |
Reaction Conditions
| Temperature | 0 °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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06864255B2 |
| Source dataset | uspto-grants-2005_03 |
| ORD ID | ord-efd3550b9fda4398976af6fd145b6557 |
| Source note | uspto-grants-2005_03 |