Sulfuric acid magnesium salt (1:1) → HCID 10162037, compound

HRID 852038Notes

Reaction equation

HRID 852038 reaction equation
[CH3:1][C:2]([CH3:27])([CH3:26])[CH2:3][N:4]([CH3:25])[C:5]1[N:10]=[C:9]([S:11][CH3:12])[N:8]=[C:7]([NH:13][C:14]2[CH:15]=[C:16]([CH:21]=[CH:22][C:23]=2[CH3:24])[C:17]([NH:19][CH3:20])=[O:18])[CH:6]=1.C(=O)(O)[O-].[Na+].[Br:33]Br.S([O-])([O-])(=O)=O.[Mg+2]>C(Cl)Cl.C(OCC)(=O)C>[Br:33][C:6]1[C:7]([NH:13][C:14]2[CH:15]=[C:16]([CH:21]=[CH:22][C:23]=2[CH3:24])[C:17]([NH:19][CH3:20])=[O:18])=[N:8][C:9]([S:11][CH3:12])=[N:10][C:5]=1[N:4]([CH2:3][C:2]([CH3:27])([CH3:26])[CH3:1])[CH3:25]

Participants

7

Procedure

To a solution of 3-{6-[(2,2-dimethyl-propyl)-methyl-amino]-2-methylsulfanyl-pyrimidin-4-ylamino}-4,N-dimethyl-benzamide (0.10 g) in methylene chloride (2 mL), was added sat. aq. sodium bicarbonate (0.05 mL) and bromine (0.013 mL). The resulting mixture was stirred at room temperature for 30 minutes, and ethyl acetate (30 mL) and magnesium sulfate (1 g) was added. After filtration and concentration, the residue was purified by silica gel column chromatography to afford the product (61.9 mg). MS (m/z): 466 (M+H).

Workup

  1. filtrationAfter filtration and concentration
  2. customthe residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-a58f1ebd13e749d99360f1000b814c98
Source dataset
uspto-grants-2007_08
Patent number
US07253174B2

Reaction notes

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