Methylamine → (2R)-(4E)-N-Methyl-5-(3-pyridyl)-4-penten-2-amine

HRID 1711506ノート

反応式

HRID 1711506 の反応式
C1(C)C=CC(S(O[C@H:11]([CH2:13]/[CH:14]=[CH:15]/[C:16]2[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=2)[CH3:12])(=O)=O)=CC=1.[CH3:23][NH2:24]>>[CH3:23][NH:24][C@@H:11]([CH2:13]/[CH:14]=[CH:15]/[C:16]1[CH:17]=[N:18][CH:19]=[CH:20][CH:21]=1)[CH3:12]

参加物

3

反応条件

温度
105 °C

実験手順

A mixture of (2S)-(4E)-5-(3-pyridyl)-4-penten-2-ol p-toluenesulfonate (3.80 g, 11.97 mmol) and methylamine (20 mL, 2.0M solution in THF) was heated at 100-110° C. for 8 h in a sealed glass tube. The mixture was cooled to ambient temperature and concentrated under reduced pressure on a rotary evaporator. The resulting brown syrup was diluted with saturated NaHCO3 solution (25 mL) and extracted with chloroform (4×25 mL). The combined chloroform extracts were dried (K2CO3), filtered, and concentrated by rotary evaporation to afford a thick, brown syrup (2.00 g). The crude product was purified by column chromatography on silica gel, eluting with chloroform-methanol (95:5, v/v). Selected fractions were combined, concentrated by rotary evaporation affording a 800 mg (37.9%) of a pale-yellow oil.

後処理

  1. temperatureThe mixture was cooled to ambient temperature
  2. concentrationconcentrated under reduced pressure on a rotary evaporator
  3. additionThe resulting brown syrup was diluted with saturated NaHCO3 solution (25 mL)
  4. extractionextracted with chloroform (4×25 mL)
  5. dry with materialThe combined chloroform extracts were dried (K2CO3)
  6. filtrationfiltered
  7. concentrationconcentrated by rotary evaporation

出典と根拠

ORDレコード
ord-594845ff8d8f46d282e296b47d7f10c1
出典データセット
uspto-grants-2010_09
特許番号
US07790757B2

反応ノート

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