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Trifluoroacetic acid → HCID 59758809, 화합물

HRID 914508
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HRID 914508 반응식
[CH3:1][C:2]([S:7][C:8]1[S:9][CH:10]=[C:11]([CH2:13][C:14]([N:16]([CH3:23])[C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=O)[N:12]=1)([CH3:6])[C:3]([OH:5])=[O:4].FC(F)(F)C(O)=O>>[CH3:6][C:2]([S:7][C:8]1[S:9][CH:10]=[C:11]([CH2:13][CH2:14][N:16]([CH3:23])[C:17]2[CH:18]=[CH:19][CH:20]=[CH:21][CH:22]=2)[N:12]=1)([CH3:1])[C:3]([OH:5])=[O:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6422Trifluoroacetic acidHCID 67400592HCID 67400592, 화합물

생성물 1

HCID 59758809HCID 59758809, 화합물

실험 절차

To the resin obtained using 2-methyl-2-[(4-{2-[methyl(phenyl)amino]-2-oxoethyl}-1,3-thiazol-2-yl)thio]propionic acid resin obtained in Example 487-1 as a starting material and by an operation similar to that of Example 461-6 was added trifluoroacetic acid (2.0 mL), and the mixture was left standing as it was for 2 hr. Then the resin was removed by filtration from the reaction mixture, and the filtrate was concentrated by blowing a nitrogen gas, vacuum dried, and purified by preparative HPLC to give the title compound (30 mg) as a pale-brown oil.

후처리

  1. customTo the resin obtained
  2. waitthe mixture was left
  3. customThen the resin was removed by filtration from the reaction mixture
  4. concentrationthe filtrate was concentrated
  5. custom
dried
  • custompurified by preparative HPLC
  • 출처 및 근거

    ORD 기록
    ord-28b7f784857d4e1d8fc5c84e62924d62
    출처 데이터셋
    uspto-grants-2011_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US08026370B2

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