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Potassium Carbonate → HCID 68496157、化合物

HRID 1038755
ノート
印刷プレビュー

反応式

HRID 1038755 の反応式
[OH:1][C:2]1[CH:10]=[C:9]2[C:5]([CH:6]=[C:7]([C:12]([OH:14])=O)[N:8]2[CH3:11])=[CH:4][CH:3]=1.[C:15]([O:19][C:20]([N:22]1[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1)=[O:21])([CH3:18])([CH3:17])[CH3:16].Cl.C(N=C=NCCCN(C)C)C.O.ON1C2C=CC=CC=2N=N1.Cl[C:52]1[CH:57]=[CH:56][C:55]([N+:58]([O-:60])=[O:59])=[CH:54][N:53]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C>[C:15]([O:19][C:20]([N:22]1[CH2:27][CH2:26][N:25]([C:12]([C:7]2[N:8]([CH3:11])[C:9]3[C:5]([CH:6]=2)=[CH:4][CH:3]=[C:2]([O:1][C:52]2[CH:57]=[CH:56][C:55]([N+:58]([O-:60])=[O:59])=[CH:54][N:53]=2)[CH:10]=3)=[O:14])[CH2:24][CH2:23]1)=[O:21])([CH3:18])([CH3:16])[CH3:17]
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 6

HCID 11430Potassium CarbonateHCID 783082-Chloro-5-nitropyridineHCID 143452tert-Butyl piperazine-1-carboxylateHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 27960291-Hydroxybenzotriazole hydrateHCID 235100986-Hydroxy-1-methyl-1H-indole-2-carboxylic acid

生成物 1

HCID 68496157HCID 68496157、化合物収率 76%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒2 回

実験手順

To a mixture of 6-hydroxy-1-methyl-1H-indole-2-carboxylic acid (12.27 g, 64.2 mmol) and piperazine-1-carboxylic acid tert-butyl ester (14.34 g, 77.0 mmol) in DMF (80 mL) were added 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (18.4 g, 96.0 mmol) and 1-hydroxybenzotriazole monohydrate (11.6 g, 75.7 mmol) under ice cooling, and the mixture was stirred at room temperature overnight. The mixture was evaporated under reduced pressure, and then water and AcOEt were added to the residue. The organic layer was separated and washed with 1M HCl, saturated aqueous NaHCO3 and brine, dried over anhydrous magnesium sulfate and evaporated. To a mixture of the residue and 2-chloro-5-nitropyridine (10.05 g, 63.4 mmol) in DMF (80 mL) was added K2CO3 (11.92 g, 86.2 mmol) and the mixture was stirred overnight at room temperature. The mixture was evaporated under reduced pressure, and then water and Et2O were added to the residual mixture. After the mixture was stirred for 1 hour, the precipitate was collected by filtration and dried to afford 23.2 g of the title compound as a yellow powder.

後処理

  1. customThe mixture was evaporated under reduced pressure
  2. additionwater and AcOEt were added to the residue
  3. customThe organic layer was separated
  4. washwashed with 1M HCl, saturated aqueous NaHCO3 and brine
  5. dry with materialdried over anhydrous magnesium sulfate
  6. customevaporated
  7. stirringthe mixture was stirred overnight at room temperature
  8. customThe mixture was evaporated under reduced pressure
  9. additionwater and Et2O were added to the residual mixture
  10. stirringAfter the mixture was stirred for 1 hour
  11. filtrationthe precipitate was collected by filtration
  12. customdried

出典と根拠

ORDレコード
ord-1cead2abede142cfab586fc9574b2d27
出典データセット
uspto-grants-2013_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08551999B2

反応ノート

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