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Hexamethyldisilazane → Ethyl 1-cyclopropyl-2,5-dimethyl-1H-imidazole-4-carboxylate

HRID 8893
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인쇄 미리보기

반응식

HRID 8893 반응식
S([O-])([O-])(=O)=O.[NH4+].[NH4+].[CH2:8]([O:10][C:11](=[O:23])[C:12]([NH:19][C:20](=O)[CH3:21])=[C:13]([NH:15][CH:16]1[CH2:18][CH2:17]1)[CH3:14])[CH3:9].C[Si](C)(C)N[Si](C)(C)C>>[CH2:8]([O:10][C:11]([C:12]1[N:19]=[C:20]([CH3:21])[N:15]([CH:16]2[CH2:18][CH2:17]2)[C:13]=1[CH3:14])=[O:23])[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 13838HexamethyldisilazaneHCID 6097028Ammonium SulfateHCID 692908002-Acetylamino-3-cyclopropylamino-but-2-enoic acid ethyl ester

생성물 1

HCID 45097089Ethyl 1-cyclopropyl-2,5-dimethyl-1H-imidazole-4-carboxylate

반응 조건

온도
145 °C

실험 절차

Fine powdered ammonium sulfate (0.13 g, 1 mmol) was added to a suspension of Z)-2-acetylamino-3-cyclopropylamino-but-2-enoic acid ethyl ester (7.0 g, 20 mmol) and hexamethyldisilazane (50 ml, 235 mmol) and refluxed over night at 145° C. The reaction mixture was evaporated and extracted with ethyl acetate and water. The organic phase was dried over sodium sulfate and evaporated. The crude product was purified by column chromatography on silica gel (ethyl acetate/methanol 4:1) and the desired compound was obtained as a light brown solid (1.3 g, 31%), MS: m/e=209.1 (M+H+).

후처리

  1. customThe reaction mixture was evaporated
  2. extractionextracted with ethyl acetate and water
  3. dry with materialThe organic phase was dried over sodium sulfate
  4. customevaporated
  5. customThe crude product was purified by column chromatography on silica gel (ethyl acetate/methanol 4:1)

출처 및 근거

ORD 기록
ord-ac2fb617a7cc49e7926340e6ef4fdd34
출처 데이터셋
uspto-grants-2006_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07091222B2

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