4-Fluorophenyl isocyanate → HCID 22936728, compound

HRID 1010121Notes

Reaction equation

HRID 1010121 reaction equation
[C:1]1([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][C:12]=2[O:13][C:14]2[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[F:21][C:22]1[CH:27]=[CH:26][C:25]([N:28]=[C:29]=[O:30])=[CH:24][CH:23]=1>C(OCC)(=O)C>[C:1]1([C:7]2[CH:8]=[N:9][CH:10]=[CH:11][C:12]=2[O:13][C:14]2[CH:15]=[CH:16][C:17]([NH:18][C:29]([NH:28][C:25]3[CH:26]=[CH:27][C:22]([F:21])=[CH:23][CH:24]=3)=[O:30])=[CH:19][CH:20]=2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1

Participants

4

Procedure

Ethyl acetate (10 ml) was added to 4-(3-phenylpyridin-4-yl)oxyaniline (84 mg, 0.32 mM), and then parafluorophenyl isocyanate (0.54 ml, 4.7 mM) was added while stirring, which was continued for 40 minutes. After adding NH type silica gel to the reaction solution, the solvent was distilled off under reduced pressure to adsorb the reaction product onto the silica gel. The silica gel was charged into a dry column packed with NH type silica gel, for column purification (chloroform:methanol=10:1). After adding ethyl acetate and n-hexane to the obtained residue, the solvent was distilled off under reduced pressure to obtain the target compound (82 mg) as a light yellow amorphous substance.

Workup

  1. additionAfter adding NH type silica gel to the reaction solution
  2. distillationthe solvent was distilled off under reduced pressure
  3. additionThe silica gel was charged into a dry column
  4. custompacked with NH type silica gel, for column purification (chloroform:methanol=10:1)
  5. additionAfter adding ethyl acetate and n-hexane to the obtained residue
  6. distillationthe solvent was distilled off under reduced pressure

Sources & evidence

ORD record
ord-e79f5f87434b4ae0ba293b75b0ba2a15
Source dataset
uspto-grants-2011_07
Patent number
US07973160B2

Reaction notes

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