Pyridine → Methyl 3-(4-(2-acetylhydrazinecarbonyl)phenoxy)-5-(benzyloxy)benzoate

HRID 2098333노트

반응식

HRID 2098333 반응식
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]([CH:22]=[C:23]([C:25]([O:27][CH3:28])=[O:26])[CH:24]=1)[O:12][C:13]1[CH:21]=[CH:20][C:16]([C:17]([OH:19])=O)=[CH:15][CH:14]=1)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.C(Cl)(=O)C(Cl)=O.[C:35]([NH:38][NH2:39])(=[O:37])[CH3:36].N1C=CC=CC=1>C(Cl)Cl.CN(C=O)C.Cl>[C:35]([NH:38][NH:39][C:17]([C:16]1[CH:20]=[CH:21][C:13]([O:12][C:11]2[CH:22]=[C:23]([CH:24]=[C:9]([O:8][CH2:1][C:2]3[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=3)[CH:10]=2)[C:25]([O:27][CH3:28])=[O:26])=[CH:14][CH:15]=1)=[O:19])(=[O:37])[CH3:36]

참가 물질

8

실험 절차

To a stirring solution of 4-[3-(benzyloxy)-5-(methoxycarbonyl)phenoxy]benzoic acid (Intermediate 11) (34 g, 82.87 mmol, 1 equiv) in dry DCM (50 mL), DMF (1.5 mL, catalytic) was added followed by oxalyl chloride (20.1 g, 158.7 mmol, 2 equiv.) dropwise at 0-5° C. The reaction mixture was stirred at room temperature for 2 h. After 2 h, a mixture of acetic hydrazide (8.8 g, 119 mmol, 1.5 equiv.) and dry pyridine (12.4 mL, 158.7 mmol, 2 equiv.) in dry DCM (50 mL) was added to the above prepared acid chloride at 0° C. The reaction mixture was allowed to warm to room temperature and stirred for 15 min. The reaction was monitored by TLC. After completion, the reaction mixture was diluted with dil. HCl and extracted with DCM. The organic layer was washed with water, brine and dried over sodium sulphate and concentrated to afford white solid. (32 g).

후처리

  1. waitAfter 2 h
  2. additionwas added to the
  3. temperatureto warm to room temperature
  4. stirringstirred for 15 min
  5. extractionextracted with DCM
  6. washThe organic layer was washed with water, brine
  7. dry with materialdried over sodium sulphate
  8. concentrationconcentrated
  9. customto afford white solid

출처 및 근거

ORD 기록
ord-58a2becd330e4cebb08eba1b24fcef9b
출처 데이터셋
uspto-grants-2013_05
특허 번호
US08450494B2

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