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HCID 117608159, 화합물 → HCID 117608156, 화합물

HRID 58826
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HRID 58826 반응식
[C:1]([O:5][C:6]([NH:8][C@@H:9]([CH2:14][CH:15]([CH2:20][C:21]#[N:22])[C:16]([O:18][CH3:19])=[O:17])[C:10]([O:12][CH3:13])=[O:11])=[O:7])([CH3:4])([CH3:3])[CH3:2]>CC(O)=O.[Pd]>[NH2:22][CH2:21][CH2:20][CH:15]([CH2:14][C@H:9]([NH:8][C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[C:10]([O:12][CH3:13])=[O:11])[C:16]([O:18][CH3:19])=[O:17]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 117608159HCID 117608159, 화합물

생성물 1

HCID 117608156HCID 117608156, 화합물

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 176Acetic Acid용매

실험 절차

To a solution of (2S)-dimethyl 2-((tert-butoxycarbonyl)amino)-4-(cyanomethyl)pentanedioate (10.0 g, 31.8 mmol) in AcOH (240 mL) was added 10% Pd/C (2.0 g) and the mixture was stirred under H2 atmosphere (70 psi) for 3 h. The mixture was filtered through a pad of Celite and the filtrate was evaporated under reduced pressure. The residue was treated with MTBE and evaporated again to afford (4S)-dimethyl 2-(2-aminoethyl)-4-((tert-butoxycarbonyl)amino)pentanedioate (crude) as a light pink solid.

후처리

  1. filtrationThe mixture was filtered through a pad of Celite
  2. customthe filtrate was evaporated under reduced pressure
  3. additionThe residue was treated with MTBE
  4. customevaporated again

출처 및 근거

ORD 기록
ord-d94b408e53a44352a3f772e60a7cbba4
출처 데이터셋
uspto-grants-2016_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09434761B2

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