Pyridine → N-(t-butyloxycarbonyl)-4-(n-hexadecylamino)benzoyl-imidazole

HRID 2163775

反応式

HRID 2163775 の反応式
[CH2:1]([NH:17][C:18]1[CH:26]=[CH:25][C:21]([C:22]([OH:24])=O)=[CH:20][CH:19]=1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16].O1CCOCC1.[C:33]([O:37][C:38]([N:40]=[N+]=[N-])=[O:39])([CH3:36])([CH3:35])[CH3:34].[N:43]1[CH:48]=CC=[CH:45][CH:44]=1>>[C:33]([O:37][C:38]([N:40]1[CH:45]=[CH:44][N:43]=[C:48]1[C:22](=[O:24])[C:21]1[CH:20]=[CH:19][C:18]([NH:17][CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH2:12][CH2:13][CH2:14][CH2:15][CH3:16])=[CH:26][CH:25]=1)=[O:39])([CH3:36])([CH3:35])[CH3:34]

参加物

5

反応物 4

HCID 1049PyridineHCID 312751,4-DioxaneHCID 472634-(Hexadecylamino)benzoic acidHCID 61256Carbonazidic acid, 1,1-dimethylethyl ester

生成物 1

HCID 20437338N-(t-butyloxycarbonyl)-4-(n-hexadecylamino)benzoyl-imidazole

実験手順

A solution of 10 g. of 4-(n-hexadecylamino)benzoic acid in 100 ml. dioxane is treated with 4.0 g. of t-butylazidoformate and 10 ml. pyridine. After stirring at room temperature for 18 hours, the protected amido-acid is precipitated from solution by addition of 150 ml. of water. The product is collected and thoroughly dried. The crude product is dissolved in 200 ml. of a mixture consisting of methylene chloride/dimethoxy ethane/pyridine (1:4:1), and to this is added 5.4 g. of 1,1'-carbonyldiimidazoye. The solution is stirred overnight at room temperature and the solvents are evaporated to yield the title compound as a thick, orange oil.

後処理

  1. customthe protected amido-acid is precipitated from solution by addition of 150 ml
  2. customThe product is collected
  3. customthoroughly dried
  4. dissolutionThe crude product is dissolved in 200 ml
  5. additionto this is added 5.4 g
  6. stirringThe solution is stirred overnight at room temperature
  7. customthe solvents are evaporated

出典と根拠

ORDレコード
ord-a75204e4a3324afebe27ec426a429862
出典データセット
uspto-grants-1979_01
特許番号
US04136256

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