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Trifluoroacetic acid → HCID 86597225、化合物

HRID 2424557
ノート
印刷プレビュー

反応式

HRID 2424557 の反応式
C(O)(C(F)(F)F)=O.[CH3:8][CH:9]([CH3:27])[CH2:10][CH2:11][NH:12][C:13]([C:15]1[N:16]=[N:17][C:18]([N:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)=[CH:19][CH:20]=1)=[O:14].[F:28][C:29]([F:37])([F:36])[CH2:30][CH:31]([CH3:35])[C:32](O)=[O:33].N12CCCN=C1CCCCC2.CN(C)CCCN=C=NCC>CN(C=O)C.C(OCC)(=O)C>[CH3:8][CH:9]([CH3:27])[CH2:10][CH2:11][NH:12][C:13]([C:15]1[N:16]=[N:17][C:18]([N:21]2[CH2:26][CH2:25][N:24]([C:32](=[O:33])[CH:31]([CH3:35])[CH2:30][C:29]([F:37])([F:36])[F:28])[CH2:23][CH2:22]2)=[CH:19][CH:20]=1)=[O:14]
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 5

HCID 6422Trifluoroacetic acidHCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 27755364,4,4-Trifluoro-2-methylbutanoic acidHCID 668493226-Piperazin-1-yl-pyridazin-3-carboxylic acid (3-methylbutyl)amide

生成物 1

HCID 86597225HCID 86597225、化合物
収率 77%

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide溶媒HCID 8857Ethyl Acetate溶媒

実験手順

A mixture of TFA salt of 6-piperazin-1-yl-pyridazine-3-carboxylic acid (3-methylbutyl)amide (100 mg, 0.25 mmol), 4,4,4-trifluoro-2-methylbutyric acid (47.8 mg, 0.31 mmol), 1,8-diazabicylco[5.4.0]undec-7-ene (77.8 mg, 0.51 mmol) and 1-hydroxy-benozotriazole hydrate (41.4 mg, 0.31 mmol) in DMF (2 mL) was stirred at ambient temperature for 15 minutes. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide (47.6 mg, 0.31 mmol) was added to this solution. The reaction mixture was stirred at ambient temperature overnight and then diluted with ethyl acetate (50 mL) and washed with aqueous saturated NaHCO3 (2×20 mL) and finally with brine (2×20 mL). The organic extract was dried over anhydrous Na2SO4, concentrated, and then purified by column chromatography eluted with hexanesethyl acetate (1:2). The product was obtained as a white flaky solid (80 mg, 75% yield). 1H NMR (300 MHz, CDCl3) δ 8.07, 7.85, 7.01, 3.60-4.00, 3.50, 3.15, 2.80, 2.21, 1.70, 1.50, 1.25, 0.95. MS (ES+) m/z 41 (M+1).

後処理

  1. stirringThe reaction mixture was stirred at ambient temperature overnight
  2. washwashed with aqueous saturated NaHCO3 (2×20 mL) and finally with brine (2×20 mL)
  3. extractionThe organic extract
  4. dry with materialwas dried over anhydrous Na2SO4
  5. concentrationconcentrated
  6. custompurified by column chromatography
  7. washeluted with hexanesethyl acetate (1:2)

出典と根拠

ORDレコード
ord-0ac47391da3448e08f2860ac993f8ccb
出典データセット
uspto-grants-2011_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07964591B2

反応ノート

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