Trifluoroacetic acid → Methyl 2-((5-bromopyridin-2-yl)amino)acetate

HRID 1825967Notes

Reaction equation

HRID 1825967 reaction equation
C(O)(C(F)(F)F)=O.[Br:8][C:9]1[CH:10]=[CH:11][C:12]([N:15](C(OC(C)(C)C)=O)[CH2:16][C:17]([O:19][CH3:20])=[O:18])=[N:13][CH:14]=1>C(Cl)Cl>[Br:8][C:9]1[CH:10]=[CH:11][C:12]([NH:15][CH2:16][C:17]([O:19][CH3:20])=[O:18])=[N:13][CH:14]=1

Participants

4

Reactant 2

HCID 6422Trifluoroacetic acidHCID 22139000Methyl 2-[(5-bromopyridin-2-yl)[(tert-butoxy)carbonyl]amino]acetate

Product 1

HCID 22139049Methyl 2-((5-bromopyridin-2-yl)amino)acetateYield 100.4%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

A 50% solution of TFA in CH2Cl2 (200 mL) was added to 5-bromo-2-[N-(tert-butoxycarbonyl)-N-(methoxycarbonylmethyl)amino]pyridine (16.5 g, 46 mmole). After stirring for 45 min the reaction was concentrated to dryness, and the residue was diluted with 1.0 N Na2CO3 (300 mL). The mixture was extracted with EtOAc (300 mL), and the organic layer was washed with brine, dried (Na2SO4), and concentrated to dryness under vacuum. The title compound (11.32 g, 100%) was obtained as a white solid: 1H NMR (400 MHz, CDCl3) δ 8.13 (d, J=2.3 Hz, 1 H), 7.48 (dd, 1 H), 6.40 (d, J=8.8 Hz, 1 H), 4.95 (br s, 1H), 4.12 (d, J=5.5 Hz, 2 H), 3.78 (s, 3H).

Workup

  1. concentrationwas concentrated to dryness
  2. additionthe residue was diluted with 1.0 N Na2CO3 (300 mL)
  3. extractionThe mixture was extracted with EtOAc (300 mL)
  4. washthe organic layer was washed with brine
  5. dry with materialdried (Na2SO4)
  6. concentrationconcentrated to dryness under vacuum

Sources & evidence

ORD record
ord-547834d0894442c9854063e6849cf782
Source dataset
uspto-grants-2006_05
Patent number
US07049310B2

Reaction notes

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