Trifluoroacetic acid → 5-(1H-pyrrol-1-yl)pyridin-3-amine

HRID 1620065Notes

Reaction equation

HRID 1620065 reaction equation
C(O)(C(F)(F)F)=O.C(OC(=O)[NH:14][C:15]1[CH:16]=[N:17][CH:18]=[C:19]([N:21]2[CH:25]=[CH:24][CH:23]=[CH:22]2)[CH:20]=1)(C)(C)C>C(Cl)(Cl)Cl>[N:21]1([C:19]2[CH:20]=[C:15]([NH2:14])[CH:16]=[N:17][CH:18]=2)[CH:22]=[CH:23][CH:24]=[CH:25]1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 89546780tert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamate

Product 1

HCID 665215025-(1H-pyrrol-1-yl)pyridin-3-amineYield 104.1%

Reagents, catalysts & solvents 1

HCID 6212ChloroformSolvent

Procedure

TFA (1 ml) was added to a chloroform (1 ml) solution containing tert-butyl(5-(1H-pyrrol-1-yl)pyridin-3-yl)carbamate (36 mg) obtained in the 1st step, followed by stirring at room temperature for 1 hour. Then, the solvent was distilled away under reduced pressure and the residue was added to a mixture of chloroform, water, and a 1M sodium hydroxide aqueous solution, followed by extraction with chloroform. The resultant was dried over anhydrous sodium sulfate, the solvent was distilled away under reduced pressure, and a light brown solid of 5-(1H-pyrrol-1-yl)pyridin-3-amine (23 mg) was thus obtained.

Workup

  1. customobtained in the 1st step
  2. distillationThen, the solvent was distilled away under reduced pressure
  3. additionthe residue was added to a mixture of chloroform, water
  4. extractiona 1M sodium hydroxide aqueous solution, followed by extraction with chloroform
  5. dry with materialThe resultant was dried over anhydrous sodium sulfate
  6. distillationthe solvent was distilled away under reduced pressure

Sources & evidence

ORD record
ord-3b4216ed278f494397d14a80b9195d52
Source dataset
uspto-grants-2014_07
Patent number
US08772320B2

Reaction notes

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