3-Aminobenzamide → 3-{[(4-Bromophenoxy)acetyl]amino}benzamide

HRID 1945386

Reaktionsgleichung

Reaktionsgleichung von HRID 1945386
[Br:1][C:2]1[CH:12]=[CH:11][C:5]([O:6][CH2:7][C:8]([OH:10])=O)=[CH:4][CH:3]=1.[NH2:13][C:14]1[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=1)[C:17]([NH2:19])=[O:18].Cl.C(NCCCN=C=NCC)C.ON1C2C=CC=CC=2N=N1.C(N(CC)C(C)C)(C)C>CN(C=O)C>[Br:1][C:2]1[CH:3]=[CH:4][C:5]([O:6][CH2:7][C:8]([NH:13][C:14]2[CH:15]=[C:16]([CH:20]=[CH:21][CH:22]=2)[C:17]([NH2:19])=[O:18])=[O:10])=[CH:11][CH:12]=1

Komponenten

7

Edukt 5

HCID 16453-AminobenzamideHCID 74657p-Bromophenoxyacetic acidHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 866015281-(3-Ethylaminopropyl)-3-ethylcarbodiimide hydrochloride

Produkt 1

HCID 173978023-{[(4-Bromophenoxy)acetyl]amino}benzamideAusbeute 21,52 %

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a mixture of (4-bromo-phenoxyacetic acid (392.5 mg, 1.8 mmol), 3-amino-benzamide (408.2 mg, 3.0 mmol), N-(3-ethylaminopropyl)-N′-ethyl carbodiimide HCl (EDC) (517.6 mg, 2.7 mmol) and 1-hydroxybenzotriazole (HOBt) (365.3 mg, 2.7 mmol) in DMF (18 mL) was added N,N-diisopropylethylamine, redistilled (DIPEA) (0.47 ml, 2.7 mmol). The mixture was stirred overnight and then partitioned between ethyl acetate and water. The organic phase was washed with brine, dried (MgSO4 anh), and concentrated. The residue was purified by recrystallization from the mixture of Ethyl acetate and MeOH to give 3-[2-(4-bromo-phenoxy)acetyl-amino]-benzamide as a white solid (134.9 mg, 21.52% yield).

Aufarbeitung

  1. distillationredistilled (DIPEA) (0.47 ml, 2.7 mmol)
  2. custompartitioned between ethyl acetate and water
  3. washThe organic phase was washed with brine
  4. dry with materialdried (MgSO4 anh)
  5. concentrationconcentrated
  6. customThe residue was purified by recrystallization from the mixture of Ethyl acetate and MeOH

Quellen und Nachweise

ORD-Eintrag
ord-2bf3b5ca4dc64704b75dad322be49c28
Quelldatensatz
uspto-grants-2013_03
Patentnummer
US08394799B2

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