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N,N,N',N'-Tetramethylethylenediamine → {1-[tert-Butyl(dimethyl)silyl]-5-fluoro-1H-indol-4-yl}boronic acid

HRID 2278387
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HRID 2278387 반응식
[Si:1]([N:8]1[C:16]2[C:11](=[CH:12][C:13]([F:17])=[CH:14][CH:15]=2)[CH:10]=[CH:9]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2].CN(CCN(C)C)C.[Li]C(CC)C.[B:31](OC(C)C)([O:36]C(C)C)[O:32]C(C)C>C1COCC1.C1CCCCC1.O>[Si:1]([N:8]1[C:16]2[C:11](=[C:12]([B:31]([OH:36])[OH:32])[C:13]([F:17])=[CH:14][CH:15]=2)[CH:10]=[CH:9]1)([C:4]([CH3:7])([CH3:6])[CH3:5])([CH3:3])[CH3:2]
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참가 물질

8

반응물 4

HCID 8037N,N,N',N'-TetramethylethylenediamineHCID 21531Triisopropyl borateHCID 594182201-(tert-butyldimethylsilyl)-5-fluoro-1H-indoleHCID 178418400CID 53628100

생성물 1

HCID 57417002{1-[tert-Butyl(dimethyl)silyl]-5-fluoro-1H-indol-4-yl}boronic acid수율 20.7%

시약·촉매·용매 3

HCID 962
Water
용매
HCID 8028Tetrahydrofuran용매
HCID 8078Cyclohexane용매

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온도
-78 °C

실험 절차

To a mixture of the product of Step 1 (4.98 g, 20 mmol) and TMEDA (2.32 g, 20 mmol) in THF at −78° C. was slowly added a 1.3M solution of s-BuLi (15.4 mL, 20 mmol) in cyclohexane and the mixture was stirred for 2 h at −78° C. Triisopropyl borate (3.76 g, 20 mmol) was added to the mixture at −78° C. and stirred for another 1 h and then warmed to −20° C. Water was added and the mixture was extracted with EtOAc and the organic layer was dried over Na2SO4 and evaporated. The residue was re-crystallized (EtOAc and n-hexane) to give the title compound (1.2 g, 20.7%).

후처리

  1. stirringstirred for another 1 h
  2. temperaturewarmed to −20° C
  3. extractionthe mixture was extracted with EtOAc
  4. dry with materialthe organic layer was dried over Na2SO4
  5. customevaporated
  6. customThe residue was re-crystallized (EtOAc and n-hexane)

출처 및 근거

ORD 기록
ord-acbecb1c68394dcabecf931a52a1896f
출처 데이터셋
uspto-grants-2015_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09133180B2

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