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Water → HCID 58392224, 화합물

HRID 561371
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HRID 561371 반응식
Br[CH2:2][C:3]1[CH:4]=[CH:5][CH:6]=[C:7]2[C:11]=1[N:10]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH:9]=[CH:8]2.[CH3:19][S-:20].[Na+].O>CN(C)C=O>[C:15]([O:14][C:12]([N:10]1[C:11]2[C:7](=[CH:6][CH:5]=[CH:4][C:3]=2[CH2:2][S:20][CH3:19])[CH:8]=[CH:9]1)=[O:13])([CH3:18])([CH3:17])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 962WaterHCID 4378561Sodium methanethiolateHCID 21874701tert-Butyl 7-(bromomethyl)-1H-indole-1-carboxylate

생성물 1

HCID 58392224HCID 58392224, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

160 mg (516 μmmol) of the compound from Example 6A and 36.2 mg (516 μmol) of sodium methanethiolate were stirred in 5 ml of dimethylformamide at RT for three days. Water was then added, and the mixture was extracted with ethyl acetate. The organic phase was dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate gradient) to result in 64 mg (45% of theory) of the title compound.

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후처리

  1. extractionthe mixture was extracted with ethyl acetate
  2. dry with materialThe organic phase was dried over magnesium sulfate
  3. filtrationfiltered
  4. concentrationconcentrated
  5. customThe residue was purified by flash chromatography (mobile phase: cyclohexane/ethyl acetate gradient)

출처 및 근거

ORD 기록
ord-c05c3154dfa5483b9f7922ec019d8c5b
출처 데이터셋
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08063234B2

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