ホームMCPワークベンチSkills
ホームワークベンチ通知マイページ
llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
  1. ホーム
  2. /反応

Sodium Chloride → N-(2-dimethylamino-ethyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxamide

HRID 1969994
ノート
印刷プレビュー

反応式

HRID 1969994 の反応式
ON1C2C=CC=CC=2N=N1.Cl.C(N=C=NCCCN(C)C)C.CN1CCOCC1.[CH3:30][N:31]([CH3:35])[CH2:32][CH2:33][NH2:34].[O:36]=[C:37]1[C:46]2[NH:47][CH:48]=[C:49]([C:50](O)=[O:51])[C:45]=2[C:44]2[CH:43]=[CH:42][CH:41]=[CH:40][C:39]=2[NH:38]1.[Cl-].[Na+]>CN(C)C=O.C(OCC)(=O)C>[CH3:30][N:31]([CH3:35])[CH2:32][CH2:33][NH:34][C:50]([C:49]1[C:45]2[C:44]3[CH:43]=[CH:42][CH:41]=[CH:40][C:39]=3[NH:38][C:37](=[O:36])[C:46]=2[NH:47][CH:48]=1)=[O:51]
参加物実験手順後処理出典と根拠反応ノート

参加物

9

反応物 6

HCID 5234Sodium ChlorideHCID 79724-MethylmorpholineHCID 66053N,N-DimethylethylenediamineHCID 757711-HydroxybenzotriazoleHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 120650844-oxo-3H,4H,5H-pyrrolo[2,3-c]quinoline-1-carboxylic acid

生成物 1

HCID 15605162
N-(2-dimethylamino-ethyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxamide
収率 13.2%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

49 mg (0.36 mmol) of 1-hydroxybenzotriazole, 69 mg (0.36 mmol) of 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride, 73 μL (0.66 mmol) of N-methylmorpholine and 40 μL (0.36 mmol) of N,N-dimethylethylenediamine are added to 75 mg (0.33 mmol) of 4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxylic acid (synthesis 75) suspended in 0.7 ml of anhydrous dimethylformamide. The reaction mixture is stirred overnight at room temperature. The mixture is diluted with ethyl acetate (20 mL) and a saturated solution of sodium chloride (20 mL). The two phases are separated and the aqueous phase is extracted with ethyl acetate (3×20 mL). The organic phases are combined, washed with n aqueous solution of potassium carbonate (10%) (3×40 mL), water (40 mL) and a saturated solution of sodium chloride (50 mL), dried over magnesium sulfate and evaporated. The residue obtained is triturated in diethyl ether to give 13 mg (13%) of N-(2-dimethylamino-ethyl)-4-oxo-4,5-dihydro-3H-pyrrolo[2,3-c]quinoline-1-carboxamide in the form of a light brown solid.

後処理

  1. customThe two phases are separated
  2. extractionthe aqueous phase is extracted with ethyl acetate (3×20 mL)
  3. washwashed with n aqueous solution of potassium carbonate (10%) (3×40 mL), water (40 mL)
  4. dry with materiala saturated solution of sodium chloride (50 mL), dried over magnesium sulfate
  5. customevaporated
  6. customThe residue obtained
  7. customis triturated in diethyl ether

出典と根拠

ORDレコード
ord-22c304326af9449cbad2b5402534a2bd
出典データセット
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08426437B2

反応ノート

読み込み中…

このページの内容参加物実験手順後処理出典と根拠反応ノート