Dichloromethane → Diisopropylethylamine

HRID 421227

반응식

HRID 421227 반응식
[C:1]([N:8]1[CH2:13][CH2:12]O[CH2:10][CH:9]1[C:14]([OH:16])=[O:15])([O:3]C(C)(C)C)=O.[CH3:17]N(C(O[N:25]1N=N[C:27]2C=CC=C[C:26]1=2)=[N+](C)C)C.[B-](F)(F)(F)F.[CH:39]([N:42]([CH:45]([CH3:47])[CH3:46])[CH2:43][CH3:44])([CH3:41])[CH3:40].[Cl:48]CCl>>[ClH:48].[CH3:17][O:16][C:14](=[O:15])[C@@H:9]([CH3:10])[NH2:8].[CH:39]([N:42]([CH:45]([CH3:47])[CH3:46])[CH2:43][CH3:44])([CH3:41])[CH3:40].[CH3:27][C@@H:26]1[C:1](=[O:3])[N:8]2[CH2:13][CH2:12][NH:42][CH2:10][CH:9]2[C:14](=[O:16])[NH:25]1

참가 물질

7

실험 절차

To a solution of N-boc-morpholine-3-carboxylic acid (2 g, 9.379 mmol) in 60 mL of dichloromethane and was added TBTU (3.313 g, 10.32 mmol) and diisopropylethyl amine (1.96 mL, 11.25 mmol). The reaction was stirred for 30 min. In the meantime, a solution of D-alanine methyl ester hydrochloride (1.93 g, 18.76 mmol) and diisopropylethylamine (3.27 mL, 18.76 mmol) in 20 mL of dichloromethane was prepared and finally added to the reaction mixture. The reaction was left stirring at room temperature for 2 h. UPLC-MS analysis showed the expected product (peak at 0.60 min, m/z=317 (M+1), 261 (M−t-Bu+1), 217 (M−Boc+1)). The reaction was diluted with dichloromethane and extracted with sat. NaHCO3, dried (Na2SO4), and the solvent removed. The crude (5.56 g) was taken to the next step without further purification.

후처리

  1. additionfinally added to the reaction mixture
  2. waitThe reaction was left
  3. stirringstirring at room temperature for 2 h
  4. extractionextracted with sat. NaHCO3
  5. dry with materialdried (Na2SO4)
  6. customthe solvent removed
  7. customThe crude (5.56 g) was taken to the next step without further purification

출처 및 근거

ORD 기록
ord-fca0426383df493bb055573c88de7bea
출처 데이터셋
uspto-grants-2012_01
특허 번호
US08097618B2

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