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Potassium Carbonate → Ethyl alpha-[(9-amino-1,2,3,4-tetrahydroacridin-8-yl)oxy]butyrate hydrate

HRID 981936
ノート
印刷プレビュー

反応式

HRID 981936 の反応式
Cl.[OH:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:16]=1[C:15]([NH2:17])=[C:14]1[C:9]([CH2:10][CH2:11][CH2:12][CH2:13]1)=[N:8]2.[C:18](=O)([O-])[O-].[K+].[K+].[CH3:24][O:25][C:26](=[O:31])[CH:27](Br)[CH2:28][CH3:29]>CN(C)C=O.O>[OH2:2].[NH2:17][C:15]1[C:16]2[C:7]([N:8]=[C:9]3[C:14]=1[CH2:13][CH2:12][CH2:11][CH2:10]3)=[CH:6][CH:5]=[CH:4][C:3]=2[O:2][CH:27]([CH2:28][CH3:29])[C:26]([O:25][CH2:24][CH3:18])=[O:31]
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 11430Potassium CarbonateHCID 95577Butanoic acid, 2-bromo-, methyl esterHCID 136404540HCID 136404540、化合物

生成物 1

HCID 67757092Ethyl alpha-[(9-amino-1,2,3,4-tetrahydroacridin-8-yl)oxy]butyrate hydrate

試薬・触媒・溶媒 2

HCID 962Water溶媒HCID 6228Dimethylformamide
溶媒

実験手順

To a solution of 8-hydroxy-1,2,3,4-tetrahydro-9-acridinamine hydrochloride (23.08 g) in dry dimethylformamide was added potassium carbonate (28.75 g), with stirring. After one hr, methyl-2-bromobutyrate (15.89 ml) was added dropwise and stirring was continued overnight. The reaction mixture was diluted with water (1.5 l), and extracted with ethyl acetate (2 l). The organic extracts were dried over anhydrous magnesium sulfate, filtered, and the filtrate was concentrated. The residue was flash chromatographed (ethyl, acetate, 5% triethylamine/ethyl acetate) to yield 30.34 g of ethyl α-[(9-amino-1,2,3,4-tetrahydroacridin-8-yl)oxy]butyrate hydrate.

後処理

  1. stirringstirring
  2. waitwas continued overnight
  3. extractionextracted with ethyl acetate (2 l)
  4. dry with materialThe organic extracts were dried over anhydrous magnesium sulfate
  5. filtrationfiltered
  6. concentrationthe filtrate was concentrated
  7. customchromatographed (ethyl, acetate, 5% triethylamine/ethyl acetate)

出典と根拠

ORDレコード
ord-82679f9fb56c49248de3067ea0a58cf5
出典データセット
uspto-grants-1991_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04994452

反応ノート

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