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Water → 2-(2-Aminopurin-9-yl)methyl butan-1,4-diol

HRID 864987
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HRID 864987 반응식
[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:11][CH:12]([CH2:17][C:18](OC)=[O:19])[C:13](OC)=[O:14])=[CH:4][N:3]=1.[BH4-].[Li+].O>C(O)(C)(C)C>[NH2:1][C:2]1[N:10]=[C:9]2[C:5]([N:6]=[CH:7][N:8]2[CH2:11][CH:12]([CH2:17][CH2:18][OH:19])[CH2:13][OH:14])=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4148881Lithium borohydrideHCID 19027589Dimethyl (2-aminopurin-9-ylmethyl)succinate

생성물 1

HCID 146200082-(2-Aminopurin-9-yl)methyl butan-1,4-diol

시약·촉매·용매 1

HCID 6386tert-Butanol용매

실험 절차

To a solution of crude dimethyl (2-aminopurin-9-ylmethyl)succinate (3.2 g, 10.9 mmol), dissolved in tert. butanol (250 ml) at 40° C., was added lithium borohydride (1.3 g, 60 mmol) in portions with stirring. After 1 hour at ambient temperature, water (30 ml) was added slowly and stirring continued over night. Inorganic salts were filtered and the solution evaporated to dryness. Yield of crude product was 1.6 g (50%). Chromatography on silica (chloroform+methanol 7+1) afforded pure product.

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후처리

  1. stirringstirring
  2. waitcontinued over night
  3. filtrationInorganic salts were filtered
  4. customthe solution evaporated to dryness
  5. customChromatography on silica (chloroform+methanol 7+1) afforded pure product

출처 및 근거

ORD 기록
ord-225b8e07cc1d4468948ef84dd06751ba
출처 데이터셋
uspto-grants-1996_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05565461

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