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Sibutramine → (-)-Sibutramine

HRID 2183829
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반응식

HRID 2183829 반응식
[CH3:1][CH:2]([CH2:4][CH:5]([N:17]([CH3:19])[CH3:18])[C:6]1([C:10]2[CH:11]=[CH:12][C:13]([Cl:16])=[CH:14][CH:15]=2)[CH2:9][CH2:8][CH2:7]1)[CH3:3]>C(OCC)(=O)C>[CH3:3][CH:2]([CH2:4][C@H:5]([N:17]([CH3:18])[CH3:19])[C:6]1([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)[CH2:7][CH2:8][CH2:9]1)[CH3:1]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 5210Sibutramine

생성물 1

HCID 937011(-)-Sibutramine

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매3회

실험 절차

12.3 g of racemic sibutramine was dissolved in 85 ml of ethyl acetate, L-DBTA dissolved in 85 ml of ethyl acetate was added thereto. The reaction mixture was heated under reflux, cooled to room temperature and then filtered to obtain crystals (ee: about 85%). And then, the crystals were suspended in 220 ml of ethyl acetate, and heated under reflux to obtain solids. The solids were recrystallized from 450 ml of isopropyl alcohol to obtain L-DBTA salt of (−)-sibutramine (ee: ≧99.3%). The L-DBTA salt of (−)-sibutramine was neutralized with saturated sodium bicarbonate, and then extracted with chloroform to obtain (−)-sibutramine free base.

후처리

  1. additionwas added
  2. temperatureThe reaction mixture was heated
  • temperatureunder reflux
  • filtrationfiltered
  • customto obtain crystals (ee: about 85%)
  • temperatureheated
  • temperatureunder reflux
  • customto obtain solids
  • customThe solids were recrystallized from 450 ml of isopropyl alcohol
  • 출처 및 근거

    ORD 기록
    ord-41e3c7a37d08478284aa5be43ed05d98
    출처 데이터셋
    uspto-grants-2005_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06900245B2

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