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Acetic Anhydride → 3-(4-Bromo-3,5-dimethyl-phenyl)-5-methyl-[1,2,4]oxadiazole

HRID 237667
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반응식

HRID 237667 반응식
C(O[C:5](=[O:7])[CH3:6])(=O)C.[Br:8][C:9]1[C:18]([CH3:19])=[CH:17][C:12]([C:13]([NH:15]O)=[NH:14])=[CH:11][C:10]=1[CH3:20]>N1C(C)=CC(C)=CC=1C>[Br:8][C:9]1[C:18]([CH3:19])=[CH:17][C:12]([C:13]2[N:14]=[C:5]([CH3:6])[O:7][N:15]=2)=[CH:11][C:10]=1[CH3:20]
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참가 물질

4

반응물 2

HCID 7918Acetic AnhydrideHCID 178426651HCID 178426651, 화합물

생성물 1

HCID 866973403-(4-Bromo-3,5-dimethyl-phenyl)-5-methyl-[1,2,4]oxadiazole

시약·촉매·용매 1

HCID 79532,4,6-Trimethylpyridine용매

실험 절차

Acetic anhydride (0.35 mL) is added to a solution of 4-bromo-N-hydroxy-3,5-dimethyl-benzamidine (0.30 g) in collidine (3 mL) at room temperature. The solution is stirred at room temperature for 1 h and then at 120° C. for 3 h. After cooling to room temperature, the mixture is concentrated, the residue is taken up in water and acetonitrile, and the resulting mixture is filtered. The filtrate is chromatographed on reversed phase (HPLC; acetonitrile/water/trifluoroacetic acid) to give the title compound. LC (method 11): tR=1.20 min; Mass spectrum (ESI+): m/z=267/269 (Br) [M+H]+.

후처리

  1. waitat 120° C. for 3 h
  2. temperatureAfter cooling to room temperature
  3. concentrationthe mixture is concentrated
  4. filtrationacetonitrile, and the resulting mixture is filtered
  5. customThe filtrate is chromatographed on reversed phase (HPLC; acetonitrile/water/trifluoroacetic acid)

출처 및 근거

ORD 기록
ord-8561b8dea9be49b7a965569c1cbfc304
출처 데이터셋
uspto-grants-2014_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08642585B2

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