Reaktion #1124304

ord-0af312bd7b714492b47d853f0c81f6c3

Reaktionsgleichung

COC(=O)c1ccc(C(=O)O)cc1Br
3-bromo-4-(methoxycarbonyl)benzoic acid
[Cl-].[NH4+]
NH4Cl
CN(C)C(On1nnc2cccnc21)=[N+](C)C.F[P-](F)(F)(F)(F)F
HATU
CCN(C(C)C)C(C)C
DIPEA
COC(=O)c1ccc(C(N)=O)cc1Br
methyl 2-bromo-4-carbamoylbenzoate
Ausbeute 52.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Extraktionthe mixture was extracted with DCM
  2. 2
    WaschenThe combined organic layers were washed with brine
  3. 3
    Trocknendried over Na2SO4
  4. 4
    Filtrationfiltered
  5. 5
    Einengenconcentrated under reduced pressure
  6. 6
    SonstigeThe residue was purified by column chromatography over silica gel
  7. 7
    Wascheneluted with PE-EA (3:1)

Vorschrift

A mixture of 3-bromo-4-(methoxycarbonyl)benzoic acid (2.5 g, 9.69 mmol), NH4Cl (1.04 g, 19.38 mmol), HATU (5.5 g, 14.5 mmol), and DIPEA (5.2 mL, 29.1 mmol) in DCM (50 mL) was stirred for 3 h at rt. Water was added and the mixture was extracted with DCM. The combined organic layers were washed with brine, dried over Na2SO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography over silica gel eluted with PE-EA (3:1) to give methyl 2-bromo-4-carbamoylbenzoate (1.3 g; yield 52%) as a white solid. MS: m/z=257.9 (M+1, ESI+).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08546357B2uspto-grants-2013_10