Hydrogen Bromide → HCID 66704062, compound

HRID 2261766Notes

Reaction equation

HRID 2261766 reaction equation
N([O-])=O.[Na+].[CH3:5][O:6][C:7]([C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=2N)=[CH:11][CH:10]=1)=[O:8].[BrH:24]>CS(C)=O.C(=O)([O-])[O-].[K+].[K+].O>[CH3:5][O:6][C:7]([C:9]1[CH:14]=[CH:13][C:12]([C:15]2[CH:20]=[CH:19][C:18]([O:21][CH3:22])=[CH:17][C:16]=2[Br:24])=[CH:11][CH:10]=1)=[O:8]

Participants

7

Procedure

To a solution of sodium nitrite (1.40 g) in dimethyl sulfoxide (50 mL) is added 2′-amino-4′-methoxy-biphenyl-4-carboxylic acid methyl ester (2.61 g). After 5 minutes, the reaction mixture is treated with a solution of 4.7 mL hydrobromic acid (48%) in 50 mL dimethyl sulfoxide. The reaction is allowed to stir at room temperature for 2 h. The reaction mixture is diluted with a solution of 20.0 g potassium carbonate dissolved in 400 mL water. The product is extracted five times with methylene chloride. The combined organic layers are dried over magnesium sulfate, filtered, and concentrated under reduced pressure. The residue is purified via flash chromatography eluting with hexanes/ethyl acetate (99:1 to 86:14) to afford the title compound (1.00 g, 31%) as a white solid.

Workup

  1. extractionThe product is extracted five times with methylene chloride
  2. dry with materialThe combined organic layers are dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe residue is purified via flash chromatography
  6. washeluting with hexanes/ethyl acetate (99:1 to 86:14)

Sources & evidence

ORD record
ord-39e83940b7b44907848dc85db1d91c06
Source dataset
uspto-grants-2010_12
Patent number
US07846960B2

Reaction notes

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