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Sodium methanethiolate → 3-Pyridinecarboxamide, 5-mercapto-N,N-dimethyl-

HRID 230858
ノート
印刷プレビュー

反応式

HRID 230858 の反応式
C[S-:2].[Na+].Br[C:5]1[CH:6]=[C:7]([C:11]([N:13]([CH3:15])[CH3:14])=[O:12])[CH:8]=[N:9][CH:10]=1>CN(C)C=O>[SH:2][C:5]1[CH:6]=[C:7]([C:11]([N:13]([CH3:15])[CH3:14])=[O:12])[CH:8]=[N:9][CH:10]=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

4

反応物 2

HCID 4378561Sodium methanethiolateHCID 234370495-Bromo-N,N-dimethylpyridine-3-carboxamide

生成物 1

HCID 577631833-Pyridinecarboxamide, 5-mercapto-N,N-dimethyl-収率 90.5%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

反応条件

温度
100 °C

実験手順

Sodium thiomethoxide (3 g) was added to a stirred solution of 5-bromo-N,N-dimethyl-3-pyridinecarboxamide (2.5g, WO2000055168) in N,N-dimethylformamide (40 ml) and the suspension stirred at 100° C. for 4 h. The solvent was concentrated in vacuo, the residue dissolved in 2M sodium hydroxide (35 ml) and water (50 ml), and the solution washed with chloroform (4×75 ml). The aqueous layer was acidified with 2M hydrochloric acid to pH 4 and extracted with chloroform (5×80 ml), and the combined organic layers were washed with brine (20 ml), dried over magnesium sulphate and concentrated in vacuo to give the title compound as an orange oil (1.8 g).

後処理

  1. concentrationThe solvent was concentrated in vacuo
  2. dissolutionthe residue dissolved in 2M sodium hydroxide (35 ml)
  3. washwater (50 ml), and the solution washed with chloroform (4×75 ml)
  4. extractionextracted with chloroform (5×80 ml)
  5. washthe combined organic layers were washed with brine (20 ml)
  6. dry with materialdried over magnesium sulphate
  7. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-a57ceb05a5074d88afd100135ff47684
出典データセット
uspto-grants-2009_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07566786B2

反応ノート

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