Hydrochloric Acid → 3-Chloro-5-(dihydroxyboryl)-1-(4-isopropoxyphenyl)indole-2-carboxylic acid ethyl ester

HRID 646138노트

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HRID 646138 반응식
[CH2:1]([O:3][C:4]([C:6]1[N:7]([C:17]2[CH:22]=[CH:21][C:20]([O:23][CH:24]([CH3:26])[CH3:25])=[CH:19][CH:18]=2)[C:8]2[C:13]([C:14]=1[Cl:15])=[CH:12][C:11](I)=[CH:10][CH:9]=2)=[O:5])[CH3:2].C([Mg]Cl)(C)C.[Li+].[Cl-].[B:34](OCC)([O:38]CC)[O:35]CC.Cl>C1COCC1.[Cl-].[Na+].O>[CH2:1]([O:3][C:4]([C:6]1[N:7]([C:17]2[CH:22]=[CH:21][C:20]([O:23][CH:24]([CH3:26])[CH3:25])=[CH:19][CH:18]=2)[C:8]2[C:13]([C:14]=1[Cl:15])=[CH:12][C:11]([B:34]([OH:38])[OH:35])=[CH:10][CH:9]=2)=[O:5])[CH3:2]

참가 물질

8

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온도
-40 °C

실험 절차

To solution of 3-chloro-5-iodo-1-(4-isopropoxyphenyl)-1H-indole-2-carboxylic acid ethyl ester (1.45 g, 3.0 mmol, see step (a) above) in THF (9 mL) was added i-PrMgCl×LiCl (0.95 M solution in THF; 3.26 mL, 3.1 mmol) at −40° C. over 5 min. After stirring for 15 min at −40° C., B(OEt)3 (1.56 mL, 9.0 mmol) was added. The temperature of the reaction mixture was allowed to reach 0° C. over 2 h, then HCl (2.5 M solution in water; 3.6 mL, 36 mmol) was added and stirring continued for a further 1 h at 0° C. The reaction mixture was diluted with brine (70 mL) and extracted with t-BuOMe (4×70 mL). The combined organic extracts were washed with brine (100 mL), dried over Na2SO4 and concentrated. The solid thereby obtained was washed several times with light petrol and filtered affording pure sub-title compound (1.04 g, 86%)

후처리

  1. waitto reach 0° C. over 2 h
  2. stirringstirring
  3. waitcontinued for a further 1 h at 0° C
  4. extractionextracted with t-BuOMe (4×70 mL)
  5. washThe combined organic extracts were washed with brine (100 mL)
  6. dry with materialdried over Na2SO4
  7. concentrationconcentrated
  8. customThe solid thereby obtained
  9. washwas washed several times with light petrol
  10. filtrationfiltered

출처 및 근거

ORD 기록
ord-9011f6e8f373477593836f2eee03a1d1
출처 데이터셋
uspto-grants-2010_04
특허 번호
US07705023B2

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