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Water → 3-Dimethylaminomethylene-2-oxo-2,3-dihydro-1h-indole-5-sulfonic acid

HRID 878792
ノート
印刷プレビュー

反応式

HRID 878792 の反応式
C(N[S:5]([C:8]1[CH:9]=[C:10]2[C:14](=[CH:15][CH:16]=1)[NH:13][C:12](=[O:17])[CH2:11]2)(=[O:7])=[O:6])(C)C.[CH3:18][N:19]([CH:21](OC)OC)[CH3:20].[OH2:26]>CN(C=O)C>[CH3:18][N:19]([CH:21]=[C:11]1[C:10]2[C:14](=[CH:15][CH:16]=[C:8]([S:5]([OH:6])(=[O:7])=[O:26])[CH:9]=2)[NH:13][C:12]1=[O:17])[CH3:20]
参加物実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 962WaterHCID 78373Dimethylformamide dimethyl acetalHCID 219156105-Isopropylaminosulfonyl-2-oxindole

生成物 1

HCID 909680093-Dimethylaminomethylene-2-oxo-2,3-dihydro-1h-indole-5-sulfonic acid

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

A solution of rpm281 (0.180 g, 0.708 mmol) and N,N-dimethylformamidedimethylacetal (0.125 g, 0.85 mmol, 1.2 eq) in DMF (2 ml) was stirred for 1 h at room temperature. Water (7 ml) was added and the product extracted with ethyl acetate (3×10 ml). The organic extracts were collected, dried over Na2SO4 and the solvent evaporated under reduced pressure to give a yellow solid, which was used in the next step without further purification.

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

後処理

  1. extractionthe product extracted with ethyl acetate (3×10 ml)
  2. customThe organic extracts were collected
  3. dry with materialdried over Na2SO4
  4. customthe solvent evaporated under reduced pressure
  5. customto give a yellow solid, which
  6. customwas used in the next step without further purification

出典と根拠

ORDレコード
ord-37fdaf6ffeb54a2ea737b7c242726551
出典データセット
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08987474B2

反応ノート

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