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Triethylsilane → Methyl 5-bromo-3-(tetrahydro-2H-thiopyran-4-ylmethyl)-1H-indole-7-carboxylate

HRID 656052
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HRID 656052 반응식
[S:1]1[CH2:6][CH2:5][CH:4]([CH:7]=O)[CH2:3][CH2:2]1.[Si](OS(C(F)(F)F)(=O)=O)(C)(C)C.[CH3:21][O:22][C:23]([C:25]1[CH:26]=[C:27]([Br:34])[CH:28]=[C:29]2[C:33]=1[NH:32][CH:31]=[CH:30]2)=[O:24].[SiH](CC)(CC)CC>C(Cl)Cl>[Br:34][C:27]1[CH:28]=[C:29]2[C:33](=[C:25]([C:23]([O:22][CH3:21])=[O:24])[CH:26]=1)[NH:32][CH:31]=[C:30]2[CH2:7][CH:4]1[CH2:3][CH2:2][S:1][CH2:6][CH2:5]1
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참가 물질

6

반응물 4

HCID 12052TriethylsilaneHCID 65367Trimethylsilyl triflateHCID 20143720Thiane-4-carbaldehydeHCID 24728848methyl 5-bromo-1H-indole-7-carboxylate

생성물 1

HCID 59332720Methyl 5-bromo-3-(tetrahydro-2H-thiopyran-4-ylmethyl)-1H-indole-7-carboxylate수율 44.2%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매

실험 절차

To a solution of tetrahydro-thiopyran-4-carbaldehyde (1.3 g, 9.84 mmol) in DCM (20 mL) was added TMSOTf (3.5 mL, 19.7 mmol) at 0° C. To this mixture 5-Bromo-1H-indole-7-carboxylic acid methyl ester (2.5 g, 9.84 mmol) was added. After 2 hours, Et3SiH (6.2 mL, 39.4 mmol) was added at 0° C., and stirring continued for 18 hours. The reaction mixture was quenched with sodium bicarbone solution and extracted with DCM. The combined organic layers were dried (MgSO4), concentrated, and purified by column chromatography on silica gel, giving 1.6 g (44%) of the title compound.

후처리

  1. waitcontinued for 18 hours
  2. customThe reaction mixture was quenched with sodium bicarbone solution
  3. extractionextracted with DCM
  4. dry with materialThe combined organic layers were dried (MgSO4)
  5. concentrationconcentrated
  6. custompurified by column chromatography on silica gel

출처 및 근거

ORD 기록
ord-16b2eefdec65464585665ca7220db486
출처 데이터셋
uspto-grants-2011_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08071584B2

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