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Sodium Azide → tert-butyl-{(4S)-5-azido-4-[(tert-butoxycarbonyl)amino]pentyl}carbamate

HRID 269613
ノート
印刷プレビュー

反応式

HRID 269613 の反応式
CS(O[CH2:6][C@@H:7]([NH:19][C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:8][CH2:9][CH2:10][NH:11][C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])(=O)=O.[N-:27]=[N+:28]=[N-:29].[Na+]>CN(C)C=O>[C:15]([O:14][C:12](=[O:13])[NH:11][CH2:10][CH2:9][CH2:8][C@H:7]([NH:19][C:20]([O:22][C:23]([CH3:26])([CH3:25])[CH3:24])=[O:21])[CH2:6][N:27]=[N+:28]=[N-:29])([CH3:18])([CH3:17])[CH3:16]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 2

HCID 33557Sodium AzideHCID 86601678(2S)-2,5-Bis[(tert-butoxycarbonyl)amino]pentyl methanesulphonate

生成物 1

HCID 86612278tert-butyl-{(4S)-5-azido-4-[(tert-butoxycarbonyl)amino]pentyl}carbamate

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
70 °C

実験手順

A solution of 218 mg (0.55 mmol) of (2S)-2,5-bis[(tert-butoxycarbonyl)amino]pentyl methanesulfonate (Example 84A) in 15 ml of dimethylformamide is mixed with 36 mg (0.55 mmol) of sodium azide and stirred at 70° C. for 12 h. Most of the solvent is removed by distillation in vacuo, and the residue is diluted with ethyl acetate. The mixture is washed several times with a saturated sodium bicarbonate solution, dried over magnesium sulfate and evaporated to dryness in vacuo. The product is reacted without further purification.

後処理

  1. customMost of the solvent is removed by distillation in vacuo
  2. additionthe residue is diluted with ethyl acetate
  3. washThe mixture is washed several times with a saturated sodium bicarbonate solution
  4. dry with materialdried over magnesium sulfate
  5. customevaporated to dryness in vacuo
  6. customThe product is reacted without further purification

出典と根拠

ORDレコード
ord-6e863506ecdb4d449332d90aef9ffac8
出典データセット
uspto-grants-2008_11
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07446102B2

反応ノート

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