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Methanol → Methyl 2-hydroxy-5-sulfamoylbenzoate

HRID 1820822
ノート
印刷プレビュー

反応式

HRID 1820822 の反応式
[OH:1][C:2]1[CH:10]=[CH:9][C:8]([S:11](=[O:14])(=[O:13])[NH2:12])=[CH:7][C:3]=1[C:4]([OH:6])=[O:5].[CH:15]1N=CN(C(N2C=NC=C2)=O)C=1.CO>C1COCC1>[CH3:15][O:5][C:4](=[O:6])[C:3]1[CH:7]=[C:8]([S:11](=[O:14])(=[O:13])[NH2:12])[CH:9]=[CH:10][C:2]=1[OH:1]
参加物反応条件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 887MethanolHCID 682631,1'-CarbonyldiimidazoleHCID 77312702-Hydroxy-5-sulfamoylbenzoic acid

生成物 1

HCID 14266941Methyl 2-hydroxy-5-sulfamoylbenzoate

試薬・触媒・溶媒 1

HCID 8028Tetrahydrofuran溶媒

反応条件

温度
50 °C

実験手順

To 62 mmol 2-hydroxy-5-sulfamoyl-benzoic acid in 80 ml THF was added 80 mmol CDI and the mixture heated at 50° C. for 1 h. 616 mmol methanol was then added, and the mixture was heated at 50° C. for 16 h. The mixture was then cooled to room temperature, concentrated in vacuo, and the residue chromatographed on silica gel (eluant: dichloromethane/methanol 20:1). The product containing fractions were concentrated in vacuo and the residue suspended in ethyl acetate and washed with aq NaHCO3 solution. The organic phase was dried with Na2SO4 and concentrated in vacuo to afford the title compound. MS (m/e): 230.2 ([M−H]−, 100%)

後処理

  1. temperaturethe mixture was heated at 50° C. for 16 h
  2. temperatureThe mixture was then cooled to room temperature
  3. concentrationconcentrated in vacuo
  4. customthe residue chromatographed on silica gel (eluant: dichloromethane/methanol 20:1)
  5. additionThe product containing fractions
  6. concentrationwere concentrated in vacuo
  7. washwashed with aq NaHCO3 solution
  8. dry with materialThe organic phase was dried with Na2SO4
  9. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-60b045a39ba14cd9aa06ad504ff2a7d7
出典データセット
uspto-grants-2009_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07605163B2

反応ノート

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