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

HRID 871128Notes

Reaction equation

HRID 871128 reaction equation
Cl[C:2]1[C:7]([I:8])=[CH:6][N:5]=[CH:4][N:3]=1.[F:9][C:10]([F:14])([F:13])[CH2:11][NH2:12].CCN(C(C)C)C(C)C>CCO>[I:8][C:7]1[C:2]([NH:12][CH2:11][C:10]([F:14])([F:13])[F:9])=[N:3][CH:4]=[N:5][CH:6]=1

Participants

5

Conditions

Temperature
120 °C

Procedure

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 hr 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, tr=12 min) gave the title compound (0.188 g, 0.614 mmol, 59.1% yield) as a yellow residue. ESI MS (M+H)+=303.9.

Workup

  1. temperatureto cool to room temperature
  2. customThe solvent was evaporated
  3. dissolutionThe crude material was dissolved in a minimal amount of CH2Cl2
  4. customto be chromatographed
  5. customPurification of the crude material by silica gel chromatography
  6. customan ISCO machine (24 g column, 35 mL/min, 0-90% EtOAc in hexanes over 25 min, tr=12 min)

Sources & evidence

ORD record
ord-2c4ea895e7c5486bbb3236056a04048d
Source dataset
uspto-grants-2015_03
Patent number
US08969586B2

Reaction notes

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