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Dibenzoyltartaric acid → 3-Methyl-4-piperidyl (3S,4S)-Pivalate

HRID 2267689
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HRID 2267689 반응식
[CH3:1][C@H:2]1[C@H:7]([O:8][C:9](=[O:14])[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5][NH:4][CH2:3]1.C1C=CC(C(O[C@@H](C(O)=O)[C@@H](OC(C2C=CC=CC=2)=O)C(O)=O)=O)=CC=1>CCOC(C)=O>[CH3:1][C@@H:2]1[C@@H:7]([O:8][C:9](=[O:14])[C:10]([CH3:13])([CH3:12])[CH3:11])[CH2:6][CH2:5][NH:4][CH2:3]1
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참가 물질

4

반응물 2

HCID 75969Dibenzoyltartaric acidHCID 59600263(3R,4R)-3-methylpiperidin-4-yl pivalate

생성물 1

HCID 596002413-Methyl-4-piperidyl (3S,4S)-Pivalate

시약·촉매·용매 1

HCID 8857Ethyl Acetate용매2회

실험 절차

Racemic 19 (62.7 g, 314.4 mmol) is dissolved in EtOAc (300 ml) and a solution of L-(−)-O,O′-Dibenzoyl tartaric acid (56.3 g, 157.2 mmol) in EtOAc (450 ml) is added. The formed solid is filtered off, washed with cold EtOAc and dried. It is then re-crystallized from hot methanol (400 ml). The crystals are collected and the free base is liberated by treatment with 1N—NaOH and extraction with ether.

후처리

  1. filtrationThe formed solid is filtered off
  2. washwashed with cold EtOAc
  3. customdried
  4. customIt is then re-crystallized from hot methanol (400 ml)
  5. customThe crystals are collected
  6. extractionthe free base is liberated by treatment with 1N—NaOH and extraction with ether

출처 및 근거

ORD 기록
ord-0978a5f09a774926a4307b02f9b62a0f
출처 데이터셋
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07858781B2

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