Potassium Phosphate, Tribasic → 3-(2-methoxyphenyl)methyl-N-BOC-histidine methyl ester

HRID 1194150ノート

反応式

HRID 1194150 の反応式
CS(OS(C)(=O)=O)(=O)=O.[CH3:10][O:11][C:12]1[CH:19]=[CH:18][CH:17]=[CH:16][C:13]=1[CH2:14]O.C(N(C(C)C)CC)(C)C.[CH3:29][O:30][C:31](=[O:54])[C@H:32]([CH2:41][C:42]1[N:46]=[CH:45][N:44](C(OC(C)(C)C)=O)[CH:43]=1)[NH:33][C:34]([O:36][C:37]([CH3:40])([CH3:39])[CH3:38])=[O:35].P([O-])([O-])([O-])=O.[K+].[K+].[K+]>ClCCl>[CH3:29][O:30][C:31](=[O:54])[C@H:32]([CH2:41][C:42]1[N:46]([CH2:14][C:13]2[CH:16]=[CH:17][CH:18]=[CH:19][C:12]=2[O:11][CH3:10])[CH:45]=[N:44][CH:43]=1)[NH:33][C:34]([O:36][C:37]([CH3:40])([CH3:38])[CH3:39])=[O:35]

参加物

7

反応条件

温度
0 °C

実験手順

A solution of 8 g methanesulfonic anhydride in 45 mL dichloromethane is chilled to -50° C. and treated dropwise with a solution of 6.2 mL 2-methoxybenzyl alcohol, 8.0 mL diisopropylethylamine and 45 mL dichloromethane. The resulting solution is warmed to 0° C. over 30 min and treated dropwise with 15.0 g N,1-bis-BOC-histidine methyl ester dissolved in 45 mL dichloromethane. The mixture is then heated at reflux 24 hr, poured into 400 mL 0.25M, pH=7 potassium phosphate buffer and the organic layer is separated, dried and evaporated. Chromatography on silica gel, eluting with chloroform-methanol (99:1) gives 3-(2-methoxyphenyl)methyl-N-BOC-histidine methyl ester as a gum. NMR (CDCl3) 4.96 (s,2H,NCH2Ar).

後処理

  1. temperatureThe mixture is then heated
  2. temperatureat reflux 24 hr
  3. customthe organic layer is separated
  4. customdried
  5. customevaporated
  6. washChromatography on silica gel, eluting with chloroform-methanol (99:1)

出典と根拠

ORDレコード
ord-90d12253e8ce4164badf3b1a59f4fb2b
出典データセット
uspto-grants-1989_03
特許番号
US04812462

反応ノート

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