Chloroform → Ethyl 2-chloro-5-phenylthiazole-4-carboxylate

HRID 383909

반응식

HRID 383909 반응식
N[C:2]1[S:3][C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:5]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[N:6]=1.[N+]([O-])(OCCC(C)C)=O.C(Cl)(Cl)[Cl:28].[OH-].[Na+]>CC#N>[Cl:28][C:2]1[S:3][C:4]([C:12]2[CH:17]=[CH:16][CH:15]=[CH:14][CH:13]=2)=[C:5]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[N:6]=1

참가 물질

6

실험 절차

To a solution of ethyl 2-amino-5-phenylthiazole-4-carboxylate in MeCN was added CuCl2 at 0° C., and the isoamyl nitrate was slowly added dropwise thereto, followed by stirring for 1 hour. To the reaction mixture was added CHCl3, followed by stirring at 0° C. for 2 hours and then at room temperature for 2 hours. The reaction mixture was neutralized by addition of a 1 M aqueous NaOH solution, and filtered through Celite. The filtrate was extracted with EtOAc, and the organic layer was washed with water and brine in this order and then dried over MgSO4. After concentration under reduced pressure, the residue obtained was purified by medium-pressure preparative liquid chromatography (silica gel YAMAZEN YFLC WPrep2XY, hexane:EtOAc) to obtain ethyl 2-chloro-5-phenylthiazole-4-carboxylate as a yellow oil.

후처리

  1. stirringby stirring at 0° C. for 2 hours
  2. waitat room temperature for 2 hours
  3. filtrationfiltered through Celite
  4. extractionThe filtrate was extracted with EtOAc
  5. washthe organic layer was washed with water and brine in this order
  6. dry with materialdried over MgSO4
  7. concentrationAfter concentration under reduced pressure
  8. customthe residue obtained
  9. customwas purified by medium-pressure preparative liquid chromatography (silica gel YAMAZEN YFLC WPrep2XY, hexane:EtOAc)

출처 및 근거

ORD 기록
ord-0c053e4a2d1c430b8f52df4f7ffa7ef9
출처 데이터셋
uspto-grants-2013_02
특허 번호
US08367696B2

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