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HCID 70239410, 화합물 → HCID 70239495, 화합물

HRID 565725
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HRID 565725 반응식
[CH3:1][C@H:2]([N:9]1[CH2:18][CH2:17][CH2:16][CH2:15][CH:10]1[C:11]([O:13][CH3:14])=[O:12])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1>C(OC)(C)(C)C>[CH3:1][C@H:2]([N:9]1[CH2:18][CH2:17][CH2:16][CH2:15][C@H:10]1[C:11]([O:13][CH3:14])=[O:12])[C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 70239410HCID 70239410, 화합물

생성물 1

HCID 70239495HCID 70239495, 화합물수율 44.5%

시약·촉매·용매 1

HCID 15413tert-Butyl methyl ether용매2회

실험 절차

Methyl N-[(S)-α-methylbenzyl]-(RS)-pipecolate (159 mg) was dissolved in methyl tert-butyl ether (2 ml) at room temperature. To this solution was added a mixture of (2S)-L-(−)-malic acid (120 mg) and methyl tert-butyl ether (2 ml) at room temperature and stirred. The resultant solution was allowed to stand at −20° C. for one day to form crystals. The crystals were separated by filtration and dried to yield a (2S)-L-(−)-malic acid salt of methyl N-[(S)-α-methylbenzyl]-(S)-pipecolate (70.8 mg) in an optical purity of 41% de and a yield of 29%.

후처리

  1. additionTo this solution was added
  • customto form crystals
  • customThe crystals were separated by filtration
  • customdried
  • 출처 및 근거

    ORD 기록
    ord-78d36c8b531a440c8d756829a907aed4
    출처 데이터셋
    uspto-grants-2001_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06172234B2

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