Ammonium Chloride → 3-Amino-5-(2-methoxy-ethyl)-5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid
Reaction equation
C[O:2][C:3]([C:5]1[C:10]([NH2:11])=[N:9][C:8]([NH:12][CH2:13][CH2:14][O:15][CH3:16])=[C:7]([C:17]#[C:18][Si](C)(C)C)[N:6]=1)=[O:4].CC([O-])(C)C.[K+].[NH4+].[Cl-]>C1COCC1>[NH2:11][C:10]1[N:9]=[C:8]2[N:12]([CH2:13][CH2:14][O:15][CH3:16])[CH:18]=[CH:17][C:7]2=[N:6][C:5]=1[C:3]([OH:2])=[O:4]Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of 3-amino-5-(2-methoxy-ethylamino)-6-trimethylsilanylethynyl-pyrazine-2-carboxylic acid methyl ester (487 mg, 1.51 mmol) in THF (7.6 ml) was added a suspension of KOtBu (356 mg, 3.17 mmol) in THF (7.6 ml) and the reaction mixture was stirred at r.t. for 2 h. At 0° C. solid NH4Cl (848 mg) was added and the mixture stirred for 30 min. After addition of half-saturated NH4Cl solution (15 ml) the mixture was extracted with EtOAc (2×15 ml), the pH of the aq. phase was adjusted the pH to 4 by addition of 1N HCl. The aq. phase was extracted with DCM/EtOH 9:1 (2×100 ml), the combined organic layers were dried with Na2SO4 and evaporated. The residue was filtered through a plug of silica gel (DCM/EtOH 90:10) to provide the title compound as brown powder. This material was used for coupling reactions without further purification.
Workup
- stirringthe mixture stirred for 30 min
- extractionwas extracted with EtOAc (2×15 ml)
- additionby addition of 1N HCl
- extractionThe aq. phase was extracted with DCM/EtOH 9:1 (2×100 ml)
- dry with materialthe combined organic layers were dried with Na2SO4
- customevaporated
- filtrationThe residue was filtered through a plug of silica gel (DCM/EtOH 90:10)
Sources & evidence
- ORD record
- ord-d909c39a367e452282f34c74fdc4a2a2
- Source dataset
- uspto-grants-2014_10
- Patent number
- US08865712B2
Reaction notes
Loading…