Methyl 3-aminopyrazinecarboxylate → HCID 57942622, compound

HRID 419003Notes

Reaction equation

HRID 419003 reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:10]([NH2:11])=[N:9][CH:8]=[CH:7][N:6]=1)=[O:4].[Cl:12][C:13]1[CH:18]=[CH:17][C:16]([S:19](Cl)(=[O:21])=[O:20])=[CH:15][C:14]=1[C:23]([F:26])([F:25])[F:24]>N1C=CC=CC=1.C(OCC)(=O)C>[CH3:1][O:2][C:3]([C:5]1[C:10]([NH:11][S:19]([C:16]2[CH:17]=[CH:18][C:13]([Cl:12])=[C:14]([C:23]([F:26])([F:24])[F:25])[CH:15]=2)(=[O:21])=[O:20])=[N:9][CH:8]=[CH:7][N:6]=1)=[O:4]

Participants

5

Reactant 2

HCID 72669Methyl 3-aminopyrazinecarboxylateHCID 27807194-Chloro-3-(trifluoromethyl)benzenesulfonyl Chloride

Product 1

HCID 57942622HCID 57942622, compoundYield 46.7%

Reagents, catalysts & solvents 2

HCID 1049PyridineSolvent2×HCID 8857Ethyl AcetateSolvent

Procedure

To a solution of 3-amino-pyrazine-2-carboxylic acid methyl ester (153 mg, 1.0 mmol) in 2.0 mL of pyridine was added 4-chloro-3-trifluoromethyl-benzenesulfonyl chloride (279 mg, 1.0 mmol) in 1.0 mL of pyridine. The mixture was stirred at room temperature for 16 h, diluted with 15 mL of ethyl acetate, washed twice with 1M HCl (15 mL), dried on MgSO4 and the solvent was evaporated. The product was purified on silica gel column (15% ethyl acetate in hexane) to afford 185 mg of 3-(4-chloro-3-trifluoromethyl-benzenesulfonylamino)-pyrazine-2-carboxylic acid methyl ester as white powder. MS: (M+H)/z=396.0.

Workup

  1. washwashed twice with 1M HCl (15 mL)
  2. customdried on MgSO4
  3. customthe solvent was evaporated
  4. customThe product was purified on silica gel column (15% ethyl acetate in hexane)

Sources & evidence

ORD record
ord-49e26daee1a546b39d65ad45a177d1b6
Source dataset
uspto-grants-2012_01
Patent number
US08093247B2

Reaction notes

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