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Sodium Azide → 2-[4-(Diphenylmethoxy)phenyl]-1-cyclohexyl-5-(1H-tetrazol-5-yl)-1H-benzimidazole

HRID 392961
ノート
印刷プレビュー

反応式

HRID 392961 の反応式
[Cl-].[Cl-].[Cl-].[Al+3].[N-:5]=[N+:6]=[N-:7].[Na+].[N-]=[N+]=[N-].[Al+3].[N-]=[N+]=[N-].[N-]=[N+]=[N-].[C:19]1([CH:25]([C:50]2[CH:55]=[CH:54][CH:53]=[CH:52][CH:51]=2)[O:26][C:27]2[CH:32]=[CH:31][C:30]([C:33]3[N:37]([CH:38]4[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]4)[C:36]4[CH:44]=[CH:45][C:46]([C:48]#[N:49])=[CH:47][C:35]=4[N:34]=3)=[CH:29][CH:28]=2)[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1>>[C:50]1([CH:25]([C:19]2[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=2)[O:26][C:27]2[CH:32]=[CH:31][C:30]([C:33]3[N:37]([CH:38]4[CH2:43][CH2:42][CH2:41][CH2:40][CH2:39]4)[C:36]4[CH:44]=[CH:45][C:46]([C:48]5[NH:49][N:7]=[N:6][N:5]=5)=[CH:47][C:35]=4[N:34]=3)=[CH:29][CH:28]=2)[CH:51]=[CH:52][CH:53]=[CH:54][CH:55]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 4

HCID 33557Sodium AzideHCID 6451240Aluminum(III) ChlorideHCID 21652180Aluminum azideHCID 226607932-[4-(Diphenylmethoxy)phenyl]-1-cyclohexyl-1H-benzimidazole-5-carbonitrile

生成物 1

HCID 1784203842-[4-(Diphenylmethoxy)phenyl]-1-cyclohexyl-5-(1H-tetrazol-5-yl)-1H-benzimidazole収率 20.6%

実験手順

Aluminum trichloride (33 mg, 0.247 mmol) was added to ice cold THF (4 mL). Sodium azide (48 mg, 0.744 mmol) was added and the resulting mixture was stirred under reflux for 30 min to complete the formation of the aluminum azide. Compound 8 (100 mg, 0.206 mmol) was added and the mixture stirred under reflux for 18 h. The reaction mixture was poured into ice cold dilute HCl to precipitate a solid. The solid was dissolved in DMF (2 mL) and the solution applied to a Shimadzu Prep HPLC. The product containing fractions were combined. Removal of the methanol resulted in the precipitation of 9 as a colorless solid (22.3 mg, 20.6% yield). ESI-MS m/e 527 (M=1). 1H NMR (DMSO) δ 8.33 (s, 1H), 8.20 (d, 1H, J=8.6 Hz), 8.0 (1H, d, J=7.41 Hz), 7.63 (d, 2H, J=8.7 Hz), 7.55 (d, 4H, J=7.2 Hz), 7.41-7.37 (m, 4H), 7.34-7.26 (m, 4). 6.72 (s, 1H), 4.34-4.27 (m, 1H), 2.36-2.23 (m, 2H), 1.97-1.83 (m, 4H), 1.66-1.62 (m, 1H), 1.43-1.21 (m. 3H).

後処理

  1. temperatureunder reflux for 30 min
  2. stirringthe mixture stirred
  3. temperatureunder reflux for 18 h
  4. additionThe reaction mixture was poured into ice cold dilute HCl
  5. customto precipitate a solid
  6. dissolutionThe solid was dissolved in DMF (2 mL)
  7. additionThe product containing fractions
  8. customRemoval of the methanol

出典と根拠

ORDレコード
ord-7c73f6c2d1f541cebf85bdd1129ee807
出典データセット
uspto-grants-2004_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US06803374B2

反応ノート

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