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Hydrochloric Acid → 1-[3-(Trifluoromethyl)benzenesulfonyl]piperazine

HRID 1667161
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HRID 1667161 반응식
[F:1][C:2]([F:26])([F:25])[C:3]1[CH:4]=[C:5]([S:9]([N:12]2[CH2:17][CH2:16][N:15](C(OC(C)(C)C)=O)[CH2:14][CH2:13]2)(=[O:11])=[O:10])[CH:6]=[CH:7][CH:8]=1.Cl>O1CCOCC1>[F:25][C:2]([F:1])([F:26])[C:3]1[CH:4]=[C:5]([S:9]([N:12]2[CH2:17][CH2:16][NH:15][CH2:14][CH2:13]2)(=[O:10])=[O:11])[CH:6]=[CH:7][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 313Hydrochloric AcidHCID 46180376HCID 46180376, 화합물

생성물 1

HCID 23056121-[3-(Trifluoromethyl)benzenesulfonyl]piperazine

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

실험 절차

The product from Example 84A (2.75 g, 6.97 mmol) was dissolved in dioxane (10 mL) with sonication. To the solution was added hydrochloric acid (4.0 Min dioxane) (5.23 mL, 20.92 mmol), and the reaction was allowed to stir at room temperature. After stirring for 4 hours, the reaction was concentrated. This residue was triturated with diethyl ether with sonication to give a solid which was collected by filtration to give the title compound as the hydrochloride salt.

후처리

  1. stirringAfter stirring for 4 hours
  2. concentrationthe reaction was concentrated
  3. customThis residue was triturated with diethyl ether with sonication
  4. customto give a solid which
  5. filtrationwas collected by filtration

출처 및 근거

ORD 기록
ord-6bee682f96364334b1516e344ddd6685
출처 데이터셋
uspto-grants-2011_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08044069B2

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