2-Methoxyethylamine → 3-Amino-6-bromo-5-(2-methoxy-ethylamino)-pyrazine-2-carboxylic acid methyl ester

HRID 474125

反応式

HRID 474125 の反応式
[CH3:1][O:2][C:3]([C:5]1[C:10]([NH2:11])=[N:9][C:8](Cl)=[C:7]([Cl:13])[N:6]=1)=[O:4].[CH3:14][O:15][C:16]([C:18]1[C:23]([NH2:24])=[N:22][C:21](Cl)=[C:20]([Br:26])[N:19]=1)=[O:17].[CH3:27][O:28][CH2:29][CH2:30][NH2:31].CCN(CC)CC>CN(C=O)C.O>[CH3:14][O:15][C:16]([C:18]1[C:23]([NH2:24])=[N:22][C:21]([NH:6][CH2:5][CH2:3][O:2][CH3:1])=[C:20]([Br:26])[N:19]=1)=[O:17].[CH3:1][O:2][C:3]([C:5]1[C:10]([NH2:11])=[N:9][C:8]([NH:31][CH2:30][CH2:29][O:28][CH3:27])=[C:7]([Cl:13])[N:6]=1)=[O:4]

参加物

8

実験手順

To a mixture of 3-amino-5,6-dichloro-pyrazine-2-carboxylic acid methyl ester [CAS 1458-18-0] and 3-amino-6-bromo-5-chloro-pyrazine-2-carboxylic acid methyl ester [CAS 14340-25-1] (799 mg, 3 mmol) in DMF was added 2-methoxy-ethylamine (0.31 ml, 3.6 mmol) and NEt3 (2.09 ml, 15 mmol) and the mixture was stirred at r.t. for 3.5 h. The reaction mixture was poured into water (150 ml) and extracted with toluene (2×150 ml). The organic layers were washed with half-saturated aq. sodium chloride, combined, dried with Na2SO4 and evaporated. The residue was purified by chromatography on silica gel (cyclohexane/EtOAc 100:0 to 0:100%) to provide the title compound together with 3-amino-6-chloro-5-(2-methoxy-ethylamino)-pyrazine-2-carboxylic acid methyl ester (about 1:1) as colorless solid. This mixture was used for the next step.

後処理

  1. extractionextracted with toluene (2×150 ml)
  2. washThe organic layers were washed with half-saturated aq. sodium chloride
  3. dry with materialdried with Na2SO4
  4. customevaporated
  5. customThe residue was purified by chromatography on silica gel (cyclohexane/EtOAc 100:0 to 0:100%)

出典と根拠

ORDレコード
ord-ba920ba017e64817be1e45ce0ecb7fe3
出典データセット
uspto-grants-2014_01
特許番号
US08637508B2

関連ノート

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