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Benzylamine → (S)-N-Benzyl-2-(Boc-amino)-2-phenylacetamide

HRID 1455825
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HRID 1455825 반응식
[C:1]([O:5][C:6]([NH:8][C@@H:9]([C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)[C:10]([OH:12])=O)=[O:7])([CH3:4])([CH3:3])[CH3:2].[CH2:19]([NH2:26])[C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1.CCN(C(C)C)C(C)C.C1CN([P+](Br)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F>C(Cl)Cl>[C:1]([O:5][C:6](=[O:7])[NH:8][C@H:9]([C:10](=[O:12])[NH:26][CH2:19][C:20]1[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=1)[C:13]1[CH:18]=[CH:17][CH:16]=[CH:15][CH:14]=1)([CH3:2])([CH3:3])[CH3:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 7504BenzylamineHCID 81531DiisopropylethylamineHCID 2733179PyBroPHCID 11010409(2S)-2-(((tert-butoxy)carbonyl)amino)-2-phenylacetic acid

생성물 1

HCID 12148799(S)-N-Benzyl-2-(Boc-amino)-2-phenylacetamide수율 62%

시약·촉매·용매 1

HCID 6344
Dichloromethane
용매
2회

실험 절차

(S)-tert-Butoxycarbonylamino-phenyl-acetic acid (1.00 g, 4 mmol) was dissolved in DCM (15 mL). Benzylamine (0.428 g, 4 mmol) and DIEA (0.65 g, 5 mmol) were added to the above mixture. The mixture which resulted was stirred at room temperature for a few minutes. PyBroP (2.10 g, 4.5 mmol) was added to the above solution in one portion and the reaction mixture was stirred overnight. The reaction mixture was diluted with DCM (150 mL) and washed with NaHCO3 (50 mL×2, sat.). The organic layer was collected and dried (Na2SO4) and the solvent was removed under reduced pressure. The crude product was purified by chromatography to provide the desired product (0.859, 62%).

후처리

  1. customThe mixture which resulted
  2. stirringthe reaction mixture was stirred overnight
  3. washwashed with NaHCO3 (50 mL×2, sat.)
  4. customThe organic layer was collected
  5. dry with materialdried (Na2SO4)
  6. customthe solvent was removed under reduced pressure
  7. customThe crude product was purified by chromatography

출처 및 근거

ORD 기록
ord-d96132a9c2a2471f86eed0e6f771e034
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482368B2

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