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Methyl iodide → HCID 58014019, 화합물

HRID 2357942
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HRID 2357942 반응식
I[CH3:2].[Si:3]([O:10][CH2:11][C:12]1[C:13]2[N:14]([N:20]=[C:21]([C:23]([F:26])([F:25])[F:24])[CH:22]=2)[C:15]([CH2:18][OH:19])=[CH:16][CH:17]=1)([C:6]([CH3:9])([CH3:8])[CH3:7])([CH3:5])[CH3:4]>C(#N)C.[Ag]=O>[Si:3]([O:10][CH2:11][C:12]1[C:13]2[N:14]([N:20]=[C:21]([C:23]([F:24])([F:25])[F:26])[CH:22]=2)[C:15]([CH2:18][O:19][CH3:2])=[CH:16][CH:17]=1)([C:6]([CH3:9])([CH3:7])[CH3:8])([CH3:5])[CH3:4]
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참가 물질

5

반응물 2

HCID 6328Methyl iodideHCID 58013985HCID 58013985, 화합물

생성물 1

HCID 58014019HCID 58014019, 화합물

시약·촉매·용매 2

HCID 92152Silver(II) oxide촉매HCID 6342Acetonitrile용매

실험 절차

Silver oxide (30.0 g) and iodomethane (16.1 mL) were added to a solution of the compound of Example 324 (9.53 g) in acetonitrile (300 mL). The mixture was stirred at room temperature for 85 hours. Subsequently, the mixture was filtered through Celite. The filtrate was concentrated and purified by silica gel column chromatography (hexane:ethyl acetate=15:1) to afford the title compound as a pale yellow powder (8.76 g).

후처리

  1. filtrationSubsequently, the mixture was filtered through Celite
  2. concentrationThe filtrate was concentrated
  3. custompurified by silica gel column chromatography (hexane:ethyl acetate=15:1)

출처 및 근거

ORD 기록
ord-93c21e40c6334827ac9b799d13dcd2a0
출처 데이터셋
uspto-grants-2010_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07763617B2

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