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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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Water → HCID 726326、化合物

HRID 1809961
ノート
印刷プレビュー

反応式

HRID 1809961 の反応式
[NH2:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][CH:3]=1.[CH2:12]([N:14]=[C:15]=[S:16])[CH3:13].O>C(#N)C>[CH2:12]([NH:14][C:15](=[S:16])[NH:1][C:2]1[CH:3]=[CH:4][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:10][CH:11]=1)[CH3:13]
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 962WaterHCID 10966Ethyl isothiocyanateHCID 12082Methyl 4-aminobenzoate

生成物 1

HCID 726326HCID 726326、化合物

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
80 °C

実験手順

To a solution of methyl 4-aminobenzoate (2-2) (30.2 mg, 0.20 mmol) in anhydrous acetonitrile (0.4 mL) is added ethyl isothiocyanate (2-1) (17.52 μL, 0.20 mmol) and the reaction mixture is heated at 80° C. overnight. After cooling to room temperature, the mixture is poured into water (50 mL) and extracted with ethyl acetate (EtOAc) (3×50 mL). The combined organic layers are washed with brine and dried using MgSO4. The drying agents are removed by filtration and the solvent is removed under vacuum. The resulting residue is then purified by flash column chromatography (silica gel, EtOAc/hexane, 0%-40%) to provide methyl 4-(3-ethylthioureido)benzoate (2-3).

後処理

  1. temperatureAfter cooling to room temperature
  2. extractionextracted with ethyl acetate (EtOAc) (3×50 mL)
  3. washThe combined organic layers are washed with brine
  4. customdried
  5. customThe drying agents are removed by filtration
  6. customthe solvent is removed under vacuum
  7. customThe resulting residue is then purified by flash column chromatography (silica gel, EtOAc/hexane, 0%-40%)

出典と根拠

ORDレコード
ord-87e1fef935c8443aaed448f76089c6aa
出典データセット
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08362050B2

反応ノート

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