Heptane → methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate

HRID 742064노트

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HRID 742064 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH:12][C@@H:13]([C:17]([OH:19])=[O:18])[CH:14]([CH3:16])[CH3:15])(=[O:11])=[O:10])=[CH:5][CH:4]=1.S(Cl)(Cl)=O.[CH3:24]CCCCCC>CO.C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([S:9]([NH:12][C@H:13]([CH:14]([CH3:16])[CH3:15])[C:17]([O:19][CH3:24])=[O:18])(=[O:11])=[O:10])=[CH:5][CH:4]=1

참가 물질

6

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온도
5 °C

실험 절차

To a solution of N-[4-methoxybenzenesulfonyl]-(D)-valine (8369 g, 29.13 mol) in methanol (30 L) at 5° C. is added thionyl chloride (2176 mL, 29.7 mol) over 2.5 hours. After stirring for 3 hours at 5° C., the reaction is stirred for 36 hours at room temperature. Most of the solvent is evaporated, and the crude product is dissolved in toluene (80 L). The toluene layer is then washed with water (20 L), saturated sodium bicarbonate (20 L), water again (20 L), 2N hydrochloric acid (20 L), brine (20 L), dried (Na2SO4), and the solvent is evaporated. The solid obtained is dissolved in ethyl acetate (8 L) and heptane (16 L) is added to induce crystallization. The precipitated product is collected by filtration to provide methyl 2(R)-[[4-methoxybenzenesulfonyl]amino]-3-methylbutanoate.

후처리

  1. stirringthe reaction is stirred for 36 hours at room temperature
  2. customMost of the solvent is evaporated
  3. dissolutionthe crude product is dissolved in toluene (80 L)
  4. washThe toluene layer is then washed with water (20 L), saturated sodium bicarbonate (20 L), water again (20 L), 2N hydrochloric acid (20 L), brine (20 L)
  5. dry with materialdried (Na2SO4)
  6. customthe solvent is evaporated
  7. customThe solid obtained
  8. customcrystallization
  9. filtrationThe precipitated product is collected by filtration

출처 및 근거

ORD 기록
ord-50f2adec32c14d05959b81a4942581fc
출처 데이터셋
uspto-grants-1996_09
특허 번호
US05552419

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