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3-Bromobenzoic acid → HCID 23599468, 화합물

HRID 1350887
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HRID 1350887 반응식
Cl.Cl.[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@@H:5]([NH2:11])[CH2:4]2.[Br:12][C:13]1[CH:14]=[C:15]([CH:19]=[CH:20][CH:21]=1)[C:16](O)=[O:17]>>[N:3]12[CH2:10][CH2:9][CH:6]([CH2:7][CH2:8]1)[C@@H:5]([NH:11][C:16](=[O:17])[C:15]1[CH:19]=[CH:20][CH:21]=[C:13]([Br:12])[CH:14]=1)[CH2:4]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 114563-Bromobenzoic acidHCID 12494972(R)-(+)-3-Aminoquinuclidine Dihydrochloride

생성물 1

HCID 23599468HCID 23599468, 화합물

실험 절차

Prepared by a method analogous to that described for the preparation of Intermediate 1 from (R)-1-azabicyclo[2.2.2]oct-3-ylamine dihydrochloride and 3-bromobenzoic acid; the compound was purified by chromatography on silica gel using ammoniated methanol/chloroform mixtures as the eluent. The compound was then dissolved in tetrahydrofuran, excess hydrogen chloride (1M solution in diethyl ether) was added, and the solution was evaporated and then recrystallised from methanol/diethyl ether to give the hydrochloride salt of the title compound as a colourless solid; MS (ES+) 309, 311 (MH+).

후처리

  1. customPrepared by a method analogous to
  2. customthe compound was purified by chromatography on silica gel using ammoniated methanol/chloroform mixtures as the eluent
  3. dissolution
The compound was then dissolved in tetrahydrofuran
  • additionexcess hydrogen chloride (1M solution in diethyl ether) was added
  • customthe solution was evaporated
  • customrecrystallised from methanol/diethyl ether
  • 출처 및 근거

    ORD 기록
    ord-5d075c9cf6ed41d7ab85adb2114f3f8b
    출처 데이터셋
    uspto-grants-2007_05
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07214688B2

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