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3-Bromobenzoic acid → HCID 23599468、化合物

HRID 891433
ノート
印刷プレビュー

反応式

HRID 891433 の反応式
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
参加物実験手順後処理出典と根拠反応ノート

参加物

3

反応物 2

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

生成物 1

HCID 23599468HCID 23599468、化合物

実験手順

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+).

後処理

  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
  • 出典と根拠

    ORDレコード
    ord-3efcf02470b040dfbcad545353fb9a65
    出典データセット
    uspto-grants-2006_02
    DOI
    10.6084/m9.figshare.5104873.v1
    特許番号
    US07001914B2

    反応ノート

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