Bromine → 2-bromo-4-methylaminosulfonylmethyl-N-trifluoroacetylaniline

HRID 745014Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 745014
[CH3:1][NH:2][S:3]([CH2:6][C:7]1[CH:19]=[CH:18][C:10]([NH:11][C:12](=[O:17])[C:13]([F:16])([F:15])[F:14])=[CH:9][CH:8]=1)(=[O:5])=[O:4].C(=O)(O)[O-].[Na+].[Br:25]Br>CO.C(Cl)Cl>[Br:25][C:9]1[CH:8]=[C:7]([CH2:6][S:3]([NH:2][CH3:1])(=[O:5])=[O:4])[CH:19]=[CH:18][C:10]=1[NH:11][C:12](=[O:17])[C:13]([F:16])([F:15])[F:14]

Komponenten

6

Edukt 3

HCID 24408BromineHCID 516892Sodium BicarbonateHCID 199702154-Methylaminosulfonylmethyl-N-trifluoroacetylaniline

Produkt 1

HCID 110032962-bromo-4-methylaminosulfonylmethyl-N-trifluoroacetylanilineAusbeute 29,7 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 887MethanolLösungsmittelHCID 6344DichloromethaneLösungsmittel2×

Versuchsvorschrift

To a chilled suspension of 4-methylaminosulfonylmethyl-N-trifluoroacetylaniline (10.9 g) in methanol (100 mL) was added sodium bicarbonate (28 g), followed by bromine (18.3 g) in methylene chloride (30 mL). The reaction mixture was then diluted with methylene chloride (70 mL) and quenched by the addition of sodium sulfite (20 g), filtered through CELITE and concentrated in vacuo to a yellow residual solid. This solid was twice reslurried in methylene chloride (300 mL) then refiltered and the filtrates evaporated in vacuo. The residual materials were combined in 10% acetone/methylene chloride solution and concentrated then purified by column chromatography (eluting with 4% acetone in methylene chloride) to give the title compound (4.10 g) mp 170° C.; TLC (methylene chloride/acetone 15:1) Rf=0.36, and the corresponding dibromide (5.56 g) TLC (methylene chloride/acetone 15:1) Rf=0.31.

Aufarbeitung

  1. customquenched by the addition of sodium sulfite (20 g)
  2. filtrationfiltered through CELITE
  3. concentrationconcentrated in vacuo to a yellow residual solid
  4. customthe filtrates evaporated in vacuo
  5. concentrationconcentrated
  6. customthen purified by column chromatography (eluting with 4% acetone in methylene chloride)

Quellen und Nachweise

ORD-Eintrag
ord-60131c72727e4532bd5b8279066dcf8c
Quelldatensatz
uspto-grants-1996_09
Patentnummer
US05559246

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