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Hydrochloric Acid → 1-(2-Piperazin-1-yl-thiazol-5-yl)-propan-1-one hydrochloride

HRID 1352395
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HRID 1352395 반응식
C(OC([N:8]1[CH2:13][CH2:12][N:11]([C:14]2[S:15][C:16]([C:19](=[O:22])[CH2:20][CH3:21])=[CH:17][N:18]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.[ClH:23]>O1CCOCC1.CCOCC>[ClH:23].[N:11]1([C:14]2[S:15][C:16]([C:19](=[O:22])[CH2:20][CH3:21])=[CH:17][N:18]=2)[CH2:12][CH2:13][NH:8][CH2:9][CH2:10]1
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참가 물질

5

반응물 2

HCID 313Hydrochloric AcidHCID 684069214-(5-Propionyl-thiazol-2-yl)-piperazine-1-carboxylic acid tert-butyl ester

생성물 1

HCID 211001701-(2-Piperazin-1-yl-thiazol-5-yl)-propan-1-one hydrochloride수율 99%

시약·촉매·용매 2

HCID 3283Diethyl Ether용매HCID 312751,4-Dioxane용매

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온도
90 °C

실험 절차

To a solution of 0.58 mmol 4-(5-propionyl-thiazol-2-yl)-piperazine-1-carboxylic acid tert-butyl ester in 6 ml dioxane was added dropwise 8.76 mmol hydrogen chloride solution (4 M in dioxane) and the mixture was stirred at 90° C. for 90 min. The reaction mixture was then cooled to 0° C. and diluted with ether. The resulting crystals were collected by filtration and washed with ether to afford the title compound as a white crystalline solid (yield 99%). MS (m/e): 226.4 (M+H+, 100%).

후처리

  1. temperatureThe reaction mixture was then cooled to 0° C.
  2. filtrationThe resulting crystals were collected by filtration
  3. washwashed with ether

출처 및 근거

ORD 기록
ord-79927b84f3bc43a7872b882ef43ced0b
출처 데이터셋
uspto-grants-2007_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07220744B2

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