Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1969893Generated: October 30, 2026

Ethanamine, 2,2,2-trifluoro- → HCID 67216455, compound

https://huagongshe.com/reaction/1969893

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
Reactant1,1'-CarbonyldiimidazoleHCID 68263—
ReactantHCID 67216364HCID 67216364—
SolventDimethylformamideHCID 6228—
ProductHCID 67216455HCID 67216455—

Reaction Conditions

Temperature65 °C

Reaction Steps

To a solution of 2,2,2-trifluoroethanamine (0.080 g, 0.804 mmol) in DMF (3 mL) was added CDI (0.150 g, 0.926 mmol). The resulting solution was stirred at about 65° C. for about 2 h. 1-((cis)-4-ethylpyrrolidin-3-yl)-6-tosyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazine (0.250 g, 0.609 mmol) was added and the reaction continued stirring at about 65° C. for about 2 h. The reaction was cooled to about ambient temperature. The solvent was removed under reduced pressure. The crude material was purified by flash chromatography on silica gel eluting with a gradient of 0-10% MeOH in afford (cis)-3-ethyl-4-(6-tosyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyrazin-1-yl)-N-(2,2,2-trifluoroethyl)pyrrolidine-1-carboxamide (0.306 g, 94%) as a brown residue: LC/MS (Table 1, Method a) Rt=2.19 min; MS m/z: 536 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08426411B2
Source datasetuspto-grants-2013_04
ORD IDord-9e31d51112584d05aa85fa4b471a4ae4
Source noteuspto-grants-2013_04