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Hydroxylamine → 1-[2-(Hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine

HRID 1582051
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인쇄 미리보기

반응식

HRID 1582051 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([N:8]2[CH2:13][CH2:12][N:11]([S:14](/[CH:17]=[CH:18]/[C:19]3[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=3)(=[O:16])=[O:15])[CH2:10][CH2:9]2)=[CH:4][CH:3]=1.[NH2:25][OH:26]>C1COCC1>[OH:26][NH:25][CH:18]([C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][CH:24]=1)[CH2:17][S:14]([N:11]1[CH2:12][CH2:13][N:8]([C:5]2[CH:4]=[CH:3][C:2]([F:1])=[CH:7][CH:6]=2)[CH2:9][CH2:10]1)(=[O:16])=[O:15]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 787HydroxylamineHCID 882266Styryl[4-(4-fluorophenyl)piperazino] sulfone

생성물 1

HCID 111764211-[2-(Hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 1-(4-fluorophenyl)-4-(trans-β-styrenesulfonyl)piperazine (620 mg, 1.79 mmol) in THF (20 ml) was added hydroxylamine (3 ml, 50% aqueous solution). The mixture was stirred for 18 hours. The solvent was evaporated. The residue was dissolved in dichloromethane and washed with water. The organic layer was dried on MgSO4 to give 1-[2-(hydroxyamino)-2-phenylethanesulfonyl]-4-(4-fluorophenyl)piperazine (730 mg).

후처리

  1. customThe solvent was evaporated
  2. dissolutionThe residue was dissolved in dichloromethane
  3. washwashed with water
  4. customThe organic layer was dried on MgSO4

출처 및 근거

ORD 기록
ord-bd69f4efa3494947a57dded1471587ec
출처 데이터셋
uspto-grants-2004_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06734184B1

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