Hydrochloric Acid → tert-Butyl (2-carbamoylfuran-3-yl)carbamate

HRID 32595

반응식

HRID 32595 반응식
C([N:4](C(C)C)CC)(C)C.C1CN([P+](ON2N=NC3C=CC=CC2=3)(N2CCCC2)N2CCCC2)CC1.F[P-](F)(F)(F)(F)F.[Cl-].[NH4+].[C:45]([O:49][C:50]([NH:52][C:53]1[CH:57]=[CH:56][O:55][C:54]=1[C:58]([OH:60])=O)=[O:51])([CH3:48])([CH3:47])[CH3:46].Cl>CN(C=O)C>[NH2:4][C:58]([C:54]1[O:55][CH:56]=[CH:57][C:53]=1[NH:52][C:50](=[O:51])[O:49][C:45]([CH3:48])([CH3:47])[CH3:46])=[O:60]

참가 물질

7

실험 절차

Diisopropylethylamine (14.75 mL) was added to a suspension of PyBOP (10.4 g), ammonium chloride (1.81 g) and 3-[(tert-butoxycarbonyl)amino]-2-furoic acid (Intermediate 81) (3.83 g) in DMF (50 mL). The resulting mixture was stirred at ambient temperature for 90 minutes, poured into 0.4 M HCl (250 mL) and extracted into DCM (3×100 mL). The combined organics were washed with water (80 mL) and brine (80 mL), dried (MgSO4), and evaporated The product was purified by flash chromatography on silica, eluting with 20-70% EtOAc in isohexane to afford the title compound as a white solid (3.38 g, 89%);

후처리

  1. extractionextracted into DCM (3×100 mL)
  2. washThe combined organics were washed with water (80 mL) and brine (80 mL)
  3. dry with materialdried (MgSO4)
  4. customevaporated The product
  5. customwas purified by flash chromatography on silica
  6. washeluting with 20-70% EtOAc in isohexane

출처 및 근거

ORD 기록
ord-fc69a7ca2cf04a67bc09dcf34db3ae30
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07427616B2

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