Ammonium Chloride → 3-Amino-5-(2-methoxy-ethyl)-5H-pyrrolo[2,3-b]pyrazine-2-carboxylic acid

HRID 538389Notes

Reaction equation

HRID 538389 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

5

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

  1. stirringthe mixture stirred for 30 min
  2. extractionwas extracted with EtOAc (2×15 ml)
  3. additionby addition of 1N HCl
  4. extractionThe aq. phase was extracted with DCM/EtOH 9:1 (2×100 ml)
  5. dry with materialthe combined organic layers were dried with Na2SO4
  6. customevaporated
  7. 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

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