Hydrochloric Acid → 6-Acetyl-3-amino-pyrazine-2-carboxylic acid methyl ester
Reaction equation
[CH3:1][O:2][C:3]([C:5]1[C:10]([NH:11]C(OC(C)(C)C)=O)=[N:9][CH:8]=[C:7]([C:19](=[O:21])[CH3:20])[N:6]=1)=[O:4].Cl>O1CCOCC1>[CH3:1][O:2][C:3]([C:5]1[C:10]([NH2:11])=[N:9][CH:8]=[C:7]([C:19](=[O:21])[CH3:20])[N:6]=1)=[O:4]Participants
4
Procedure
To a stirred solution of 6-acetyl-3-tert-butoxycarbonylamino-pyrazine-2-carboxylic acid methyl ester (500 mg, 1.69 mmol) at rt in dioxane (10 ml) under an argon atmosphere was added 4 M HCl solution in dioxane (4.23 ml, 16.9 mmol) in one portion. The reaction mixture was stirred overnight, then concentrated. The residue was triturated with Et2O, filtrated and dried. The solid was taken up in EtOAc (50 ml) and washed with saturated aqueous Na2CO3 solution (20 ml) and brine. The organic phase was dried over MgSO4, filtrated and concentrated to give the title compound (313 mg, 95%) as orange powder.
Workup
- concentrationconcentrated
- customThe residue was triturated with Et2O
- filtrationfiltrated
- customdried
- washwashed with saturated aqueous Na2CO3 solution (20 ml) and brine
- dry with materialThe organic phase was dried over MgSO4
- filtrationfiltrated
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-8e77add58169400b8350ef2ce5722fea
- Source dataset
- uspto-grants-2014_01
- Patent number
- US08623866B2
Reaction notes
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