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Piperidine → {(S)-1-[(S)-2-((2S,4S)-4-Amino-2-benzylcarbamoyl-pyrrolidin-1-yl)-1-cyclohexyl-2-oxo-ethylcarbamoyl]-ethyl}-methyl-carbamic acid tert-butyl ester

HRID 1481923
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인쇄 미리보기

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HRID 1481923 반응식
C1C2C(COC(=O)[NH:17][C@H:18]3[CH2:22][C@@H:21]([C:23](=[O:32])[NH:24][CH2:25][C:26]4[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=4)[N:20]([C:33](=[O:55])[C@@H:34]([NH:41][C:42](=[O:54])[C@@H:43]([N:45]([C:47]([O:49][C:50]([CH3:53])([CH3:52])[CH3:51])=[O:48])[CH3:46])[CH3:44])[CH:35]4[CH2:40][CH2:39][CH2:38][CH2:37][CH2:36]4)[CH2:19]3)C3C(=CC=CC=3)C=2C=CC=1.N1CCCCC1>CN(C=O)C>[C:50]([O:49][C:47](=[O:48])[N:45]([C@H:43]([C:42](=[O:54])[NH:41][C@@H:34]([CH:35]1[CH2:36][CH2:37][CH2:38][CH2:39][CH2:40]1)[C:33]([N:20]1[CH2:19][C@@H:18]([NH2:17])[CH2:22][C@H:21]1[C:23](=[O:32])[NH:24][CH2:25][C:26]1[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1)=[O:55])[CH3:44])[CH3:46])([CH3:51])([CH3:52])[CH3:53]
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참가 물질

4

반응물 2

HCID 8082PiperidineHCID 118677385((3S,5S)-5-benzylcarbamoyl-1-{(S)-2-[(S)-2-(tert-butoxycarbonyl-methyl-amino)-propionylamino]-2-cyclohexyl-acetyl}-pyrrolidin-3-yl)-carbamic acid 9H-fluoren-9-ylmethyl ester

생성물 1

HCID 90231684{(S)-1-[(S)-2-((2S,4S)-4-Amino-2-benzylcarbamoyl-pyrrolidin-1-yl)-1-cyclohexyl-2-oxo-ethylcarbamoyl]-ethyl}-methyl-carbamic acid tert-butyl ester수율 100.5%

시약·촉매·용매 1

HCID 6228
Dimethylformamide
용매

실험 절차

((3S,5S)-5-Benzylcarbamoyl-1-{(S)-2-[(S)-2-(tert-butoxycarbonyl-methyl-amino)-propionylamino]-2-cyclohexyl-acetyl}-pyrrolidin-3-yl)-carbamic acid 9H-fluoren-9-ylmethyl ester (100 mg, 0.13 mmol) was dissolved in DMF (0.9 mL) at room temperature and piperidine (0.1 mL) was added. The mixture was stirred at room temperature for 30 minutes, concentrated and the residue purified by silica gel chromatography to give the title compound as a white foam (71 mg, 52%).

후처리

  1. concentrationconcentrated
  2. customthe residue purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-3899d05e178347c980819fa3ccfea9da
출처 데이터셋
uspto-grants-2016_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09409888B2

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