Pyridine → HCID 178481683、化合物

HRID 219716ノート

反応式

HRID 219716 の反応式
[CH:1]1([C:5](O)=O)[CH2:4][CH2:3][CH2:2]1.C(N1C=CN=C1)(N1C=CN=C1)=O.N1C=CC=CC=1.[CH3:26][NH:27][C:28](=[S:31])[NH:29][NH2:30]>CN(C)C=O>[CH3:26][N:27]1[C:5]([CH:1]2[CH2:4][CH2:3][CH2:2]2)=[N:30][N:29]=[C:28]1[SH:31]

参加物

6

実験手順

5 g of cyclobutyl carboxylic acid (49.9 mmol) were dissolved in 50 ml of dimethylformamide. Within 10 min. 12.15 g of 1,1′-carbonyldiimidazol (74.91 mmol) were added in portions. After stirring for 1 h at room temperature 23 ml of pyridin were added followed by the addition of 10.5 g of 4-methyl-3-thiosemicarbazide (99.88 mmol). The solution was stirred at room temperature for 72 h and then poured into 600 ml of ice water. Stirring was continued for 30 min. before the aqueous layer was extracted three times with 50 ml dichloromethane and three times with 50 ml ethyl acetate each. The combined organic layers were dried over magnesium sulfate, filtered, and the solvent was evaporated, thereby yielding 5.2 g of the crude title product which was used without further purification.

後処理

  1. additionwere added
  2. stirringStirring
  3. waitwas continued for 30 min. before the aqueous layer
  4. extractionwas extracted three times with 50 ml dichloromethane and three times with 50 ml ethyl acetate each
  5. dry with materialThe combined organic layers were dried over magnesium sulfate
  6. filtrationfiltered
  7. customthe solvent was evaporated

出典と根拠

ORDレコード
ord-9452eb93325c4780aea4d491fef39a77
出典データセット
uspto-grants-2012_06
特許番号
US08202868B2

反応ノート

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