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Acetonitrile → HCID 69201758, 화합물

HRID 1392962
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HRID 1392962 반응식
Br[C:2]1[S:3][C:4]([C:7]([O:9][CH3:10])=[O:8])=[CH:5][N:6]=1.[C:11]1([N:17]2[CH2:22][CH2:21][NH:20][CH2:19][CH:18]2CC)[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.C(=O)([O-])[O-].[K+].[K+].[C:31](#N)[CH3:32]>>[CH3:10][O:9][C:7]([C:4]1[S:3][C:2]([N:20]2[CH2:19][CH2:18][N:17]([CH2:11][CH2:16][C:15]3[CH:14]=[CH:13][CH:12]=[CH:32][CH:31]=3)[CH2:22][CH2:21]2)=[N:6][CH:5]=1)=[O:8]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 4

HCID 6342AcetonitrileHCID 11430Potassium CarbonateHCID 2773502Methyl 2-bromothiazole-5-carboxylateHCID 200993912-Ethyl-1-phenylpiperazine

생성물 1

HCID 69201758HCID 69201758, 화합물수율 66.4%

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온도
80 °C

실험 절차

To a solution of methyl 2-bromothiazole-5-carboxylate 1 (222 mg, 1.00 mmol) in acetonitrile (20 mL) were added N-phenyl ethyl piperazine 14e (228 mg, 1.20 mmol) and potassium carbonate (152 mg, 1.10 mmol) under a N2 atmosphere. The reaction mixture was heated to reflux at 80° C. for 10 h. The reaction mixture was filtered through Celite and the filtrate was concentrated under reduced pressure. The residue was purified by column chromatography using silica gel to give the compound 15e (245 mg, 66.4%).

후처리

  1. temperatureThe reaction mixture was heated
  2. filtrationThe reaction mixture was filtered through Celite
  3. concentrationthe filtrate was concentrated under reduced pressure
  4. customThe residue was purified by column chromatography

출처 및 근거

ORD 기록
ord-5b177eb5073240f8abd5e7308d5775fd
출처 데이터셋
uspto-grants-2008_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07345043B2

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