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Acetic Acid → HCID 19836752、化合物

HRID 1521852
ノート
印刷プレビュー

反応式

HRID 1521852 の反応式
[S:1]1[C:6]2[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=2[NH:4][C:3](=O)[CH2:2]1.C[C:13]([CH3:16])([O-:15])C.[K+].[C:18]([OH:21])(=O)[CH3:19].[CH3:22][N:23](C=O)C>O>[CH:22]1[N:4]2[C:3]([CH2:2][S:1][C:6]3[CH:7]=[CH:8][CH:9]=[CH:10][C:5]=32)=[C:19]([C:18]([O:15][CH2:13][CH3:16])=[O:21])[N:23]=1
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 4

HCID 176Acetic AcidHCID 6228Dimethylformamide2 回HCID 213964H-1,4-Benzothiazin-3-oneHCID 23665647Potassium tert-butoxide2 回

生成物 1

HCID 19836752HCID 19836752、化合物

試薬・触媒・溶媒 1

HCID 962Water溶媒

実験手順

To a solution of 2H-1,4-benzothiazin-3(4H)-one (0.7 g, 4.24 mmol, 1 eq) in DMF (20 mL) is added potassium tert- butoxide (0.50 g, 4.49 mmol, 1.06 eq) and the reaction mixture is stirred at RT for 10 min. The reaction mixture is cooled with ice and diethyl chloro phosphonate (1.1 mL, 7.63 mmol, 1.8 eq) is added and the reaction mixture is stirred at RT for 5 minutes. The reaction mixture is then cooled with ice and a solution of ethyl isocyano acetate (0.65 mL, 5.94 mmol, 1.4 eq) in DMF and potassium tert-butoxide (0.66 g, 5.93 mmol, 1.4 eq) are sequentially added and the reaction mixture is stirred at RT overnight. The reaction mixture is acidified with 10 mL of acetic acid, diluted with water and poured into ice and extracted with ethylacetate. The organic layer is dried over Na2SO4 and concentrated. The crude is purified by column chromatography to afford the title compound. 1H NMR (DMSO-d6, 400 MHz): δ 8.50 (s, 1H), 7.90-7.88 (d, J=7.3 Hz, 1H), 7.56-7.54 (m, 1H), 7.39-7.36 (m, 1H), 7.32-7.30 (m, 1H), 4.42 (s, 2H), 4.27 (q, J=7.7 Hz, 2H), 1.29 (t, J=6.6 Hz, 3H). MS (ESI+): 261.2. HPLC (max plot) 95.13%; Rt 3.62 min.

後処理

  1. additionis added
  2. stirringthe reaction mixture is stirred at RT for 5 minutes
  3. temperatureThe reaction mixture is then cooled with ice
  4. stirringthe reaction mixture is stirred at RT overnight
  5. additionpoured into ice
  6. extractionextracted with ethylacetate
  7. dry with materialThe organic layer is dried over Na2SO4
  8. concentrationconcentrated
  9. customThe crude is purified by column chromatography

出典と根拠

ORDレコード
ord-144344f1c2d84b1cb69b412e217975c2
出典データセット
uspto-grants-2015_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09073940B2

反応ノート

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