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Dimethylformamide → 4-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoyl chloride

HRID 2297540
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HRID 2297540 반응식
S(Cl)([Cl:3])=O.CN(C=O)C.[CH3:10][C:11]1[O:15][N:14]=[C:13]([C:16]2[CH:24]=[CH:23][C:19]([C:20](O)=[O:21])=[CH:18][CH:17]=2)[N:12]=1>C1(C)C=CC=CC=1>[CH3:10][C:11]1[O:15][N:14]=[C:13]([C:16]2[CH:24]=[CH:23][C:19]([C:20]([Cl:3])=[O:21])=[CH:18][CH:17]=2)[N:12]=1
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참가 물질

5

반응물 3

HCID 6228DimethylformamideHCID 24386Thionyl ChlorideHCID 71278084-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoic acid

생성물 1

HCID 71645884-(5-Methyl-1,2,4-oxadiazol-3-yl)benzoyl chloride

시약·촉매·용매 1

HCID 1140Toluene용매

실험 절차

46 ml of thionyl chloride and 1 ml of DMF are added to a solution of 10.0 g of 4-(5-methyl-1,2,4-oxadiazol-3-yl)benzoic acid in 150 ml of toluene. The solution is heated under reflux for 5 hours. The solvent is removed, giving 4-(5-methyl-1,2,4-oxadiazol-3-yl)-benzoyl chloride, EI 222. Subsequent reaction with 9.3 g of 1-tert-butoxycarbonylpiperazine in 150 ml of dichloromethane and 48 ml of triethylamine gives, after customary work-up, tert-butyl 4-[4-(5-methyl-[1,2,4]oxadiazol-3-yl)benzoyl]piperazine-1-carboxylate, FAB 373.

후처리

  1. temperatureThe solution is heated
  2. temperatureunder reflux for 5 hours
  3. customThe solvent is removed

출처 및 근거

ORD 기록
ord-59c6cfc95950462abf0e9f2aeeb426a4
출처 데이터셋
uspto-grants-2002_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06492368B1

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