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Ethanol → tert-butyl 2-(4-amino-3-(4,5-dihydro-1H-imidazol-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate

HRID 1798742
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HRID 1798742 반응식
[C:1]([O:5][C:6](=[O:20])[CH2:7][N:8]1[C:12]2=[N:13][CH:14]=[N:15][C:16]([NH2:17])=[C:11]2[C:10]([C:18]#[N:19])=[N:9]1)([CH3:4])([CH3:3])[CH3:2].CCO.[CH2:24](N)[CH2:25][NH2:26]>C(O)(=O)C>[NH2:17][C:16]1[N:15]=[CH:14][N:13]=[C:12]2[N:8]([CH2:7][C:6]([O:5][C:1]([CH3:4])([CH3:2])[CH3:3])=[O:20])[N:9]=[C:10]([C:18]3[NH:26][CH2:25][CH2:24][N:19]=3)[C:11]=12
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참가 물질

5

반응물 3

HCID 702EthanolHCID 3301EthylenediamineHCID 59242680(4-Amino-3-cyano-pyrazolo[3,4-d]pyrimidin-1-yl)-acetic acid tert-butyl ester

생성물 1

HCID 59242681tert-butyl 2-(4-amino-3-(4,5-dihydro-1H-imidazol-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate수율 90%

시약·촉매·용매 1

HCID 176Acetic Acid용매

실험 절차

To a mixture of (4-amino-3-cyano-pyrazolo[3,4-d]pyrimidin-1-yl)-acetic acid tert-butyl ester (80 g, 0.291 mol) and EtOH (800 mL) in an ice water bath was added acetic acid (67 mL) and then ethylenediamine (195 mL). The resulting mixture was refluxed for 90 min, cooled to room temperature and filtered. The solid was suspended in water (1 L), filtered and dried in vacuo to give of tert-butyl 2-(4-amino-3-(4,5-dihydro-1H-imidazol-2-yl)-1H-pyrazolo[3,4-d]pyrimidin-1-yl)acetate (84.6 g, 90% yield). MS (ES) m/z 318.1 (M+H+).

후처리

  1. temperatureThe resulting mixture was refluxed for 90 min
  2. filtrationfiltered
  3. filtrationfiltered
  4. customdried in vacuo

출처 및 근거

ORD 기록
ord-226d8017485748548e10af502a235723
출처 데이터셋
uspto-grants-2013_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08343975B2

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