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Trifluoroacetic acid → HCID 18794222, 화합물

HRID 1004045
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HRID 1004045 반응식
[CH3:1][C:2]1[NH:16][CH2:15][CH2:14][C:4]2=[C:5]3[C:10](=[N:11][C:3]=12)[CH:9]=[CH:8][C:7]([O:12][CH3:13])=[CH:6]3.[C:17](O)([C:19]([F:22])([F:21])[F:20])=[O:18]>C(N(CC)CC)C>[CH2:1]=[C:2]1[C:3]2[NH:11][C:10]3[C:5](=[CH:6][C:7]([O:12][CH3:13])=[CH:8][CH:9]=3)[C:4]=2[CH2:14][CH2:15][N:16]1[C:17](=[O:18])[C:19]([F:22])([F:21])[F:20]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 6422Trifluoroacetic acidHCID 178487038HCID 178487038, 화합물

생성물 1

HCID 18794222HCID 18794222, 화합물수율 20%

시약·촉매·용매 1

HCID 8471Triethylamine용매

실험 절차

To a solution of 10-methoxyharmalan (40 mg) in triethylamine (1 ml) is added TFA (2.2 eq). After reaction for 15 min. at 0° C., the mixture is hydrolysed and extracted with CH2Cl2. The crude product is then chromatographed on a preparative plate (eluent: CH2Cl2). 1-Methylene-2-trifluoroacetyl-6-methoxy-1,2,3,4-tetra-hydro-β-carboline is recovered (yield: 20%).

후처리

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
custom
After reaction for 15 min. at 0° C.
  • extractionextracted with CH2Cl2
  • customThe crude product is then chromatographed on a preparative plate (eluent: CH2Cl2)
  • custom1-Methylene-2-trifluoroacetyl-6-methoxy-1,2,3,4-tetra-hydro-β-carboline is recovered (yield: 20%)
  • 출처 및 근거

    ORD 기록
    ord-a539d09935db42fb9cac7bada0e57245
    출처 데이터셋
    uspto-grants-2000_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06048868

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