Di-tert-butyl dicarbonate → [2-(3,4-Dimethoxy-phenyl)-1-methyl-ethyl]-ethyl amine

HRID 2099710

반응식

HRID 2099710 반응식
Br.[CH2:2]([NH:4][CH:5]([CH3:15])[CH2:6][C:7]1[CH:8]=[C:9]([OH:14])[C:10]([OH:13])=[CH:11][CH:12]=1)[CH3:3].[C:16](=[O:19])(O)[O-].[Na+].[C:21](O[C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])(OC(C)(C)C)=O>O.C1COCC1>[CH3:21][O:14][C:9]1[CH:8]=[C:7]([CH2:6][CH:5]([NH:4][CH2:2][CH3:3])[CH3:15])[CH:12]=[CH:11][C:10]=1[O:19][CH3:16].[C:32]([O:31][C:29](=[O:30])[N:4]([CH:5]([CH3:15])[CH2:6][C:7]1[CH:12]=[CH:11][C:10]([OH:13])=[C:9]([OH:14])[CH:8]=1)[CH2:2][CH3:3])([CH3:33])([CH3:34])[CH3:35]

참가 물질

7

실험 절차

To all of 2B from the above reaction mixture was added 30 mL of 50% THF in water. To the reaction mixture 1.1 g of sodium bicarbonate was added as a solid followed by 1.35 g (6.18 mmol) of di-t-butyl dicarbonate in 7 mL of THF dropwise over a period of 30 minutes. The reaction mixture was allowed to stir at room temperature for 18 hours, then concentrated under reduced pressure. This was diluted with 50 mL of water and the pH of the solution was adjusted to 5. The aqueous layer was extracted with 3×100 mL of ethyl acetate. The organic layers were combined, dried (anhydrous Na2SO4) and concentrated to dryness. The residue was purified by silica gel column chromatography using 30% ethyl acetate in hexane to give 764 mg (2.58 mmol, 53% from 2A) of 2C as a clear gum (M+Na, 318).

후처리

  1. concentrationconcentrated under reduced pressure
  2. additionThis was diluted with 50 mL of water
  3. extractionThe aqueous layer was extracted with 3×100 mL of ethyl acetate
  4. dry with materialdried (anhydrous Na2SO4)
  5. concentrationconcentrated to dryness
  6. customThe residue was purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-f2f5e5f550ac45f092d8012c30aa23a3
출처 데이터셋
uspto-grants-2009_08
특허 번호
US07569676B2

연결된 노트

불러오는 중…