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Acetonitrile → Sodium [4-(4-Cyclopropyl-piperazine-1-carbonyl)-phenyl]-hydroxy-methanesulfonate

HRID 13562
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인쇄 미리보기

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HRID 13562 반응식
[CH:1]1([N:4]2[CH2:9][CH2:8][N:7]([C:10]([C:12]3[CH:19]=[CH:18][C:15]([CH:16]=[O:17])=[CH:14][CH:13]=3)=[O:11])[CH2:6][CH2:5]2)[CH2:3][CH2:2]1.C(#N)C.[OH:23][S:24]([O-:26])=[O:25].[Na+:27]>O>[CH:1]1([N:4]2[CH2:9][CH2:8][N:7]([C:10]([C:12]3[CH:19]=[CH:18][C:15]([CH:16]([OH:17])[S:24]([O-:26])(=[O:25])=[O:23])=[CH:14][CH:13]=3)=[O:11])[CH2:6][CH2:5]2)[CH2:2][CH2:3]1.[Na+:27]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6342AcetonitrileHCID 23665763Sodium BisulfiteHCID 592181834-(4-Cyclopropyl-piperazine-1-carbonyl)-benzaldehyde

생성물 1

HCID 59340027Sodium [4-(4-Cyclopropyl-piperazine-1-carbonyl)-phenyl]-hydroxy-methanesulfonate

시약·촉매·용매 1

HCID 962Water용매2회

반응 조건

온도
50 °C

실험 절차

A 100 mL flask was charged with 4-(4-cyclopropyl-piperazine-1-carbonyl)-benzaldehyde (2.58 g, 10.0 mmol, 1.0 eq), acetonitrile (30 mL), and water (1.0 mL) under nitrogen atmosphere. The reaction mixture was heated to 50° C. A solution of NaHSO3 (1.14 g, 11.0 mol, 1.1 eq) in water (2.0 mL) was added dropwise over 5 min. The reaction mixture was then cooled to 17° C. The product was collected by filtration as a white solid.

후처리

  1. temperatureThe reaction mixture was then cooled to 17° C
  2. filtrationThe product was collected by filtration as a white solid

출처 및 근거

ORD 기록
ord-1999f9fd5f3e4b5f818c084473b4137d
출처 데이터셋
uspto-grants-2010_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07728129B2

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