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Ethyl 1H-indole-3-acetate → tert-butyl 2-bromo-3-(2-ethoxy-2-oxoethyl)-1H-indole-1-carboxylate

HRID 1471643
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HRID 1471643 반응식
[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[C:3]([CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:2]1.C1C(=O)N([Br:23])C(=O)C1.CCN(C(C)C)C(C)C.[CH3:33][C:34]([O:37][C:38]([O:40]C(OC(C)(C)C)=O)=O)([CH3:36])[CH3:35]>C(Cl)Cl.CN(C1C=CN=CC=1)C>[Br:23][C:2]1[N:1]([C:38]([O:37][C:34]([CH3:36])([CH3:35])[CH3:33])=[O:40])[C:9]2[C:4]([C:3]=1[CH2:10][C:11]([O:13][CH2:14][CH3:15])=[O:12])=[CH:5][CH:6]=[CH:7][CH:8]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 13067Ethyl 1H-indole-3-acetateHCID 67184N-bromobutanimide2회HCID 81531DiisopropylethylamineHCID 90495Di-tert-butyl dicarbonate

생성물 1

HCID 90281421tert-butyl 2-bromo-3-(2-ethoxy-2-oxoethyl)-1H-indole-1-carboxylate수율 58%

시약·촉매·용매 2

HCID 14284
4-(Dimethylamino)pyridine
촉매
HCID 6344Dichloromethane용매

실험 절차

Ethyl 2-(1H-indol-3-yl)acetate (15 g, 73.9 mmol) was dissolved in DCM (750 mL). At ambient temperature, NBS (13.15 g, 73.9 mmol) was added to the reaction mixture in 5 portions approximately 2 minutes apart. After the last addition of NBS, iPr2NEt (28 mL, 162 mmol) was added slowly to the reaction mixture and stirred for 5 minutes. Boc2O (33.8 g, 155 mmol) was added followed by DMAP (900 mg). After stirring at 16 h, the reaction was partitioned between DCM and H2O. The organics were washed with aqueous 1N HCl and dried over sodium sulfate. After removal of solvent, the crude product was purified by silica gel chromatography to provide tert-butyl 2-bromo-3-(2-ethoxy-2-oxoethyl)-1H-indole-1-carboxylate (16.3 g, 58%). MS (m/z) 382 [M+H]+.

후처리

  1. additionwas added slowly to the reaction mixture
  2. stirringAfter stirring at 16 h
  3. customthe reaction was partitioned between DCM and H2O
  4. washThe organics were washed with aqueous 1N HCl
  5. dry with materialdried over sodium sulfate
  6. customAfter removal of solvent
  7. customthe crude product was purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-5919ff02e5c54d7fb44c2ac26b094108
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09012441B2

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