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Methylamine → Tyr(3-tBu)-NHMe

HRID 1383724
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HRID 1383724 반응식
[NH2:1][C@H:2]([C:15]([O:17]C)=O)[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:5]=1.[CH3:19][NH2:20].[C-]#N.[Na+]>CO>[NH2:1][C@H:2]([C:15]([NH:20][CH3:19])=[O:17])[CH2:3][C:4]1[CH:9]=[CH:8][C:7]([OH:10])=[C:6]([C:11]([CH3:14])([CH3:13])[CH3:12])[CH:5]=1
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참가 물질

5

반응물 3

HCID 6329MethylamineHCID 8929Sodium CyanideHCID 15549498Tyr(3-tBu)-OMe

생성물 1

HCID 131722741Tyr(3-tBu)-NHMe

시약·촉매·용매 1

HCID 887Methanol용매2회

실험 절차

To a solution of 10.6 g (42.0 mmol) of Tyr(3-tBu)-OMe in 80 ml of methanol, 80 ml of a solution of 40% methylamine in methanol and 0.41 g of sodium cyanide were added and the mixture was stirred at room temperature for 4 hours. The reaction mixture was concentrated under reduced pressure and the resulting residue was dissolved in methylene chloride, followed by washing first with water, then with saturated brine. The organic layer was dried with anhydrous sodium sulfate and concentrated under reduced pressure; the resulting residue was subjected to silica gel column chromatography (eluting solvent consisting of chloroform, methanol and aqueous ammonia at a ratio of 20:1:0.1) to give Tyr(3-tBu)-NHMe in the amount of 7.3 g (70%).

후처리

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. dissolutionthe resulting residue was dissolved in methylene chloride
  3. washby washing first with water
  4. dry with materialThe organic layer was dried with anhydrous sodium sulfate
  5. concentrationconcentrated under reduced pressure
  6. washeluting solvent

출처 및 근거

ORD 기록
ord-eaba3042d66f4b80b21192bae6d7a6fa
출처 데이터셋
uspto-grants-2001_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06255285B1

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