Dimethylformamide → 4Iodo-benzoic acid N'-(2,2-dimethyl-propionyl)-hydrazide

HRID 31409

반응식

HRID 31409 반응식
[I:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][CH:3]=1.C(O[C:16]([CH3:19])([CH3:18])[CH3:17])(=O)NN.C[N:21](C(ON1N=NC2C=CC=NC1=2)=[N+](C)C)C.F[P-](F)(F)(F)(F)F.ON1C2C=CC=CC=2N=N1.C(N(CC)C(C)C)(C)C.C[N:64](C)[CH:65]=[O:66]>>[CH3:17][C:16]([CH3:19])([CH3:18])[C:65]([NH:64][NH:21][C:6](=[O:8])[C:5]1[CH:4]=[CH:3][C:2]([I:1])=[CH:10][CH:9]=1)=[O:66]

참가 물질

7

실험 절차

4-Iodobenzoic acid (5 g, 20.2 mmol) was dissolved in dimethylformamide (50 ml). To this was added tert-butyl carbazate (2.66 g, 20.2 mmol), HATU (9.2 g, 24.2 mmol), 1-hydroxybenzotriazole (2.7 g, 20.2 mmol) and N,N-diisopropylethylamine (10.5 ml, 60.5 mmol). The mixture was stirred for 17 hours at room temperature. The solvent was removed in vacuo and the residue partitioned between dichloromethane (75 ml) and saturated aqueous sodium bicarbonate solution (75 ml). The organic layer was washed with water (100 ml), brine (100 ml), dried over magnesium sulfate, filtered and the solvent removed in vacuo. The desired product was obtained as a cream solid (4.6 g, 12.7 mmol).

후처리

  1. customThe solvent was removed in vacuo
  2. customthe residue partitioned between dichloromethane (75 ml) and saturated aqueous sodium bicarbonate solution (75 ml)
  3. washThe organic layer was washed with water (100 ml), brine (100 ml)
  4. dry with materialdried over magnesium sulfate
  5. filtrationfiltered
  6. customthe solvent removed in vacuo

출처 및 근거

ORD 기록
ord-42cdd1f4f85041759000fb71106a03b8
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07425555B2

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