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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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HCID 54273654, 화합물 → HCID 53896857, 화합물

HRID 1584095
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HRID 1584095 반응식
[CH3:1][O:2][C:3]1[CH:24]=[C:23]([C:25]#[N:26])[CH:22]=[CH:21][C:4]=1[CH2:5][NH:6][C:7](=[O:20])[C@@H:8]1[CH2:12][CH2:11][CH2:10][N:9]1C(OC(C)(C)C)=O>C(Cl)Cl>[CH3:1][O:2][C:3]1[CH:24]=[C:23]([C:25]#[N:26])[CH:22]=[CH:21][C:4]=1[CH2:5][NH:6][C:7](=[O:20])[C@@H:8]1[CH2:12][CH2:11][CH2:10][NH:9]1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 1

HCID 54273654HCID 54273654, 화합물

생성물 1

HCID 53896857HCID 53896857, 화합물

시약·촉매·용매 1

HCID 6344Dichloromethane용매

실험 절차

11.4 g (31.7 mmol) of Boc-proline 2-methoxy-4-cyanobenzylamide were dissolved in 130 ml of methylene chloride and, at 0-5° C., saturated with HCI [sic]. After 2 h the Boc group had been completely eliminated. The solvent was removed under reduced pressure, and the product was used without further purification in the next reaction. 1H-NMR (DMSO-d6 ; δ in ppm): 10.25 (s, 1H); 8.60 (s, 1H); 7.50 (d, 1H; 7.42 (dd, 1H); 7.39 (d, 1); 4.40-4.20 (m, 3H); 3.88 (s, 3H); 3.20 (m, 2H); 2.35 (m, 1H); 2.00-1.80 (m, 3H)

후처리

  1. customThe solvent was removed under reduced pressure
  2. customthe product was used without further purification in the next reaction

출처 및 근거

ORD 기록
ord-b02107aba18643a580b99f0e7ded057e
출처 데이터셋
uspto-grants-1999_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05932567

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