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Water → N9-(3-Azidopropyl)-2-amino-6-chloropurine

HRID 1695085
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HRID 1695085 반응식
Cl[CH2:2][CH2:3][CH2:4][N:5]1[CH:13]=[N:12][C:11]2[C:6]1=[N:7][C:8]([NH2:15])=[N:9][C:10]=2[Cl:14].[N-:16]=[N+:17]=[N-:18].[Na+].O>CS(C)=O>[N:16]([CH2:2][CH2:3][CH2:4][N:5]1[CH:13]=[N:12][C:11]2[C:6]1=[N:7][C:8]([NH2:15])=[N:9][C:10]=2[Cl:14])=[N+:17]=[N-:18]
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참가 물질

5

반응물 3

HCID 962WaterHCID 33557Sodium AzideHCID 85823850N9-(3-Chloropropyl)-2-amino-6-chloropurine

생성물 1

HCID 86067829N9-(3-Azidopropyl)-2-amino-6-chloropurine수율 24.7%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
80 °C

실험 절차

N9-(3-Chloropropyl)-2-amino-6-chlorpurine (21, 2.56 g, 10.40 mmol) and sodium azide (811 mg, 12.48 mmol) are dissolved in 25 mL DMSO and stirred at 80° C. for 16 h. After cooling to room temperature, the reaction mixture is poured into 150 mL of water and extracted with CH2Cl2. The combined organic phases are washed with water, dried over MgSO4 and evaporated in vacuo. The residue is purified by flash column chromatography (dichloromethane/methanol 50:1 to 10:1) to yield the title compound as a colorless solid (650 mg, 2.57 mmol, 24%). 1H-NMR (400 MHz, DMSO-d6): δ=8.12 (s, 1H, H-8), 6.89 (s, 2H, NH2), 4.10 (t, J=6.8, 2H, CH2), 3.38 (t, J=6.8, 2H, CH2), 2.05 (m, 2H, CH2) ppm. MS (ESI) m/z 253.0 [M+H]+.

후처리

  1. temperatureAfter cooling to room temperature
  2. extractionextracted with CH2Cl2
  3. washThe combined organic phases are washed with water
  4. dry with materialdried over MgSO4
  5. customevaporated in vacuo
  6. customThe residue is purified by flash column chromatography (dichloromethane/methanol 50:1 to 10:1)

출처 및 근거

ORD 기록
ord-5f2dec05b2c64f169eaf727ba447898c
출처 데이터셋
uspto-grants-2012_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08163479B2

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