Trifluoroacetic acid → HCID 69153779, compound

HRID 2114297Notes

Reaction equation

HRID 2114297 reaction equation
C(OC(=O)[NH:7][CH2:8][C:9](=[O:18])[N:10]([CH3:17])[C:11]1[CH:16]=[CH:15][N:14]=[CH:13][CH:12]=1)(C)(C)C.[C:20]([OH:26])([C:22]([F:25])([F:24])[F:23])=[O:21]>>[F:23][C:22]([F:25])([F:24])[C:20]([OH:26])=[O:21].[NH2:7][CH2:8][C:9]([N:10]([CH3:17])[C:11]1[CH:12]=[CH:13][N:14]=[CH:15][CH:16]=1)=[O:18]

Participants

3

Reactant 2

HCID 6422Trifluoroacetic acidHCID 59773381HCID 59773381, compound

Product 1

HCID 69153779HCID 69153779, compound

Procedure

[(Methyl-pyridin-4-yl-carbamoyl)-methyl]carbamic acid tert-butyl ester (181) (7 g, 28.1mmol) was dissolved in TFA (35mL) at rt. The reaction had to be cooled to prevent excessive heat being released. Once the reaction had settled, it was left for 1 hr. TFA was evaporated and the residue co-evaporated with toluene (3×1000 mL) and dried under vacuum to afford compound (182).

Workup

  1. temperatureto be cooled
  2. temperatureto prevent excessive heat
  3. customTFA was evaporated
  4. dry with materialthe residue co-evaporated with toluene (3×1000 mL) and dried under vacuum

Sources & evidence

ORD record
ord-a8b1ecb6ea684961aef4eff4d07cfbfe
Source dataset
uspto-grants-2008_10
Patent number
US07432379B2

Reaction notes

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