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Azobisisobutyronitrile → HCID 67143122, 화합물

HRID 1245500
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HRID 1245500 반응식
[Si:1]([O:18][CH2:19][C@H:20]1[O:24][C@@H:23]([N:25]2[CH:32]=[C:31]([CH3:33])[C:29](=[O:30])[NH:28][C:26]2=[O:27])[C@H:22]([O:34][CH2:35][CH2:36][O:37][CH3:38])[C@@H:21]1OC(OC1C=CC=C(C(C)(C)C)C=1)=S)([C:14]([CH3:17])([CH3:16])[CH3:15])([C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[C:53]1([CH:59]=[CH:60][Sn](CCCC)(CCCC)CCCC)[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=1.CC(N=NC(C#N)(C)C)(C#N)C>C1C=CC=CC=1>[Si:1]([O:18][CH2:19][C@H:20]1[O:24][C@@H:23]([N:25]2[CH:32]=[C:31]([CH3:33])[C:29](=[O:30])[NH:28][C:26]2=[O:27])[C@H:22]([O:34][CH2:35][CH2:36][O:37][CH3:38])[C@@H:21]1[CH:60]=[CH:59][C:53]1[CH:58]=[CH:57][CH:56]=[CH:55][CH:54]=1)([C:14]([CH3:17])([CH3:16])[CH3:15])([C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)[C:8]1[CH:9]=[CH:10][CH:11]=[CH:12][CH:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6547Azobisisobutyronitrile2회HCID 4372073HCID 4372073, 화합물HCID 10700230HCID 10700230, 화합물

생성물 1

HCID 67143122HCID 67143122, 화합물수율 13.6%

시약·촉매·용매 1

HCID 241Benzene용매

반응 조건

온도
40 °C

실험 절차

To a solution of 5′-O-(tert-butyldiphenylsilyl)-3′-O-(3-tert-butylphenoxythiocarbonyl)-2′-O-(2-methoxyethyl)-5-methyluridine (15.0 g, 20.0 mmol) in 150 mL of benzene was added PhCH═CHSnBu3 (18.7 g, 50 mmol). The resulting solution was degassed three times with argon at rt and 45° C. After AIBN (1.0 g, 6.1 mmol) was added, the resulting solution was refluxed for 2 h. Another portion of AIBN (1.0 g, 6.1 mmol) was added after cooling to about 40° C. and refluxed for 2 h. This procedure was repeated until the starting material disappeared. The solvent was evaporated and the residue was purified by flash chromatography on a silica gel column using 10:1 and 5:1 hexanes-EtOAc as eluent to give 1.74 g of 5′-O-(tert-butyldiphenylsilyl)-3′-deoxy-2′-O-(2-methoxyethyl)-3′-(2-phenylethenyl)5-methyluridine as a white foam.

후처리

  1. customThe resulting solution was degassed three times with argon at rt
  2. custom45° C
  3. temperaturethe resulting solution was refluxed for 2 h
  4. temperaturerefluxed for 2 h
  5. customThe solvent was evaporated
  6. customthe residue was purified by flash chromatography on a silica gel column

출처 및 근거

ORD 기록
ord-dee00ab737af42f6832be515f1060d95
출처 데이터셋
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07125855B2

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