1,2-Dichloroethane → 4-Cyano-5-(2-nitro-5-phenoxy-phenyl)-pentanoic acid cyclohexyl-methyl-amide

HRID 252463노트

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HRID 252463 반응식
[C:1]([CH:3]([CH2:9][C:10]1[CH:15]=[C:14]([O:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)[CH:13]=[CH:12][C:11]=1[N+:23]([O-:25])=[O:24])[CH2:4][CH2:5][C:6]([OH:8])=O)#[N:2].C1C=CC2N(O)N=NC=2C=1.C(N(CC)CC)C.C(Cl)CCl.[CH3:47][NH:48][CH:49]1[CH2:54][CH2:53][CH2:52][CH2:51][CH2:50]1>ClCCl>[CH:49]1([N:48]([CH3:47])[C:6](=[O:8])[CH2:5][CH2:4][CH:3]([C:1]#[N:2])[CH2:9][C:10]2[CH:15]=[C:14]([O:16][C:17]3[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=3)[CH:13]=[CH:12][C:11]=2[N+:23]([O-:25])=[O:24])[CH2:54][CH2:53][CH2:52][CH2:51][CH2:50]1

참가 물질

7

실험 절차

4-cyano-5-(2-nitro-5-phenoxy-phenyl)-pentanoic acid (0.230 g, 0.68 mmol) was dissolved in dichloromethane (1.5 mL) followed by addition of HOBt (0.103 g, 0.68 mmol), triethylamine (0.170 mL, 0.68 mmol), EDC (0.194 g, 1.01 mmol) and N-methyl-cyclohexylamine (0.09 mL, 0.68 mmol). The reaction was allowed to proceed for 16 h after which time, the solvent was removed under reduced pressure. The resulting mixture was dissolved in ethyl acetate and washed 3 times with 10% sodium carbonate solution, one time with saturated brine solution, 3 times with 1N HCl and then again one time with brine wash. The organic layer was dried with anhydrous sodium sulfate and the solvent was removed under reduced pressure to yield a residue. The residue was purified with flash chromatography using a mixture of 65:35 heptanes:ethyl acetate as the mobile phase to yield a residue.

후처리

  1. customafter which time, the solvent was removed under reduced pressure
  2. dissolutionThe resulting mixture was dissolved in ethyl acetate
  3. washwashed 3 times with 10% sodium carbonate solution, one time with saturated brine solution, 3 times with 1N HCl
  4. washagain one time with brine wash
  5. dry with materialThe organic layer was dried with anhydrous sodium sulfate
  6. customthe solvent was removed under reduced pressure
  7. customto yield a residue
  8. customThe residue was purified with flash chromatography
  9. additiona mixture of 65:35 heptanes
  10. customethyl acetate as the mobile phase to yield a residue

출처 및 근거

ORD 기록
ord-426dc85434c24783a3ba03e323e1afcf
출처 데이터셋
uspto-grants-2011_01
특허 번호
US07868022B2

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