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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1186834Generated: November 4, 2026

Ethanamine, 2,2,2-trifluoro- → 5-Iodo-N-(2,2,2-trifluoroethyl)-4-pyrimidinamine

https://huagongshe.com/reaction/1186834

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanamine, 2,2,2-trifluoro-HCID 9773—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Chloro-5-iodopyrimidineHCID 11230204—
SolventEthanolHCID 702—
Product5-Iodo-N-(2,2,2-trifluoroethyl)-4-pyrimidinamineHCID 6634188259.1%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 4-chloro-5-iodopyrimidine (0.250 g, 1.040 mmol) and 2,2,2-trifluoroethanamine (0.216 g, 2.184 mmol) in EtOH (volume: 2.080 ml) was added Hunig's Base (0.200 ml, 1.144 mmol). The reaction mixture was heated in a microwave for 4 h at 120° C. and then allowed to cool to room temperature. The solvent was evaporated. The crude material was dissolved in a minimal amount of CH2Cl2 to be chromatographed. Purification of the crude material by silica gel chromatography using an ISCO machine (24 g column, 35 mL/min, 0-90% EtOAc in hexanes over 25 min, ret. T=12 min) gave Intermediate 107A (0.188 g, 0.614 mmol, 59.1% yield) as a yellow residue. MS (ESI): m/z=303.9 [M+H]+ HPLC Peak ret. T=1.26 minutes was product. (HPLC conditions: Column:Luna C18 4.6×30 mm 3 u A:10:90 H2O:ACN NH4OAc/B:10:90 H2O:ACN NH4OAc; 0%-95% B in 2 min; 4 mL/min flow).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08673922B2
Source datasetuspto-grants-2014_03
ORD IDord-eedae6160343477aa97200d1d8ae105d
Source noteuspto-grants-2014_03