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Chloroform → 4-(Pyridin-2-ylmethyl)-1,4-diaza-bicyclo[3.2.2]nonane

HRID 1454777
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HRID 1454777 반응식
[H-].[Al+3].[Li+].[H-].[H-].[H-].[N:7]12[CH2:15][CH2:14][CH:11]([CH2:12][CH2:13]1)[N:10]([C:16]([C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][N:19]=1)=O)[CH2:9][CH2:8]2.C(Cl)(Cl)Cl.CO.C(Cl)(Cl)Cl>C1COCC1>[N:19]1[CH:20]=[CH:21][CH:22]=[CH:23][C:18]=1[CH2:16][N:10]1[CH:11]2[CH2:12][CH2:13][N:7]([CH2:15][CH2:14]2)[CH2:8][CH2:9]1
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참가 물질

6

반응물 4

HCID 6212ChloroformHCID 21226445Aluminium lithium hydrideHCID 21584188Chloroform methanolHCID 68865039(1,4-Diazabicyclo[3.2.2]non-4-yl)(pyridin-2-yl)methanone

생성물 1

HCID 114359054-(Pyridin-2-ylmethyl)-1,4-diaza-bicyclo[3.2.2]nonane

시약·촉매·용매 1

HCID 8028
Tetrahydrofuran
용매

실험 절차

To a stirred solution of lithium aluminum hydride (0.33 mL of 1M THF solution) at ambient temperature was added dropwise a solution of (1,4-diazabicyclo[3.2.2]non-4-yl)(pyridin-2-yl)methanone (120 mg, 0.52 mmol) in dry THF (2 mL). The resulting yellowish solution was stirred for 12 hours, quenched with water and aqueous NaOH, and filtered through diatomaceous earth. The filtrate was concentrated to give the product which was subjected to chromatography on silica gel eluting with an ammoniated-chloroform to 15% MeOH/chloroform gradient to give the title compound as a free base syrup (28.0 mg). MS (ES+) 218 (MH+).

후처리

  1. customquenched with water and aqueous NaOH
  2. filtrationfiltered through diatomaceous earth
  3. concentrationThe filtrate was concentrated
  4. customto give the product which

출처 및 근거

ORD 기록
ord-840824c8338a4dec95a11e948ea5fdef
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482338B2

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