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Hydrochloric Acid → benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate

HRID 1034088
ノート
印刷プレビュー

反応式

HRID 1034088 の反応式
[H-].[Na+].[C:3]([O:7][C:8]([NH:10][C:11]1[CH:12]=[C:13]([CH:31]=[CH:32][CH:33]=1)[C:14]([C:16]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[N:18]([CH2:25][CH2:26][CH2:27][C:28]([OH:30])=[O:29])[CH:17]=1)=[O:15])=[O:9])([CH3:6])([CH3:5])[CH3:4].[CH2:34](Br)[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1.Cl>CN(C)C=O>[CH2:34]([N:10]([C:11]1[CH:12]=[C:13]([CH:31]=[CH:32][CH:33]=1)[C:14]([C:16]1[C:24]2[C:19](=[CH:20][CH:21]=[CH:22][CH:23]=2)[N:18]([CH2:25][CH2:26][CH2:27][C:28]([O:30][CH2:14][C:13]2[CH:31]=[CH:32][CH:33]=[CH:11][CH:12]=2)=[O:29])[CH:17]=1)=[O:15])[C:8]([O:7][C:3]([CH3:6])([CH3:4])[CH3:5])=[O:9])[C:35]1[CH:40]=[CH:39][CH:38]=[CH:37][CH:36]=1
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

6

反応物 4

HCID 313Hydrochloric AcidHCID 7498Benzyl BromideHCID 24758Sodium hydrideHCID 190247254-[3-(3-Tert-butoxycarbonylaminobenzoyl)indol-1-yl]butyric acid

生成物 1

HCID 19024831benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate収率 96.9%

試薬・触媒・溶媒 1

HCID 6228
Dimethylformamide
溶媒

反応条件

温度
0 °C

実験手順

60% Sodium hydride in mineral oil (0.13 g) was added to a solution of 4-[3-(3-tert-butoxycarbonylaminobenzoyl)-indol-1-yl]butyric acid (0.47 g) in N,N-dimethylformamide (7 ml). The mixture was stirred at 0° C. for 1 hour. Benzyl bromide (0.95 g) was added to the mixture and the mixture was stirred at room temperature for 20 hours. The mixture was poured into ice water and 0.5N-hydrochloric acid and extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate and evaporated. The residue was chromatographed on silica gel (30 g) eluting with a mixture of n-hexane and ethyl acetate (5:1) to give benzyl 4-[3-[3-(N-benzyl-N-tert-butoxycarbonylamino)benzoyl]indol-1-yl]butyrate (325 mg) as an oil.

後処理

  1. stirringthe mixture was stirred at room temperature for 20 hours
  2. extractionextracted with ethyl acetate
  3. washThe organic layer was washed with water
  4. dry with materialdried over magnesium sulfate
  5. customevaporated
  6. customThe residue was chromatographed on silica gel (30 g)
  7. washeluting with a mixture of n-hexane and ethyl acetate (5:1)

出典と根拠

ORDレコード
ord-27f882def41e411fa821859c8bce3a91
出典データセット
uspto-grants-1994_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US05312829

反応ノート

読み込み中…

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