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Potassium Iodide → HCID 23447401, 화합물

HRID 2186182
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인쇄 미리보기

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HRID 2186182 반응식
Cl[CH2:2][S:3]([N:6]1[CH2:11][CH2:10][N:9]([CH2:12][C:13]2[CH:18]=[CH:17][C:16]([C:19]#[N:20])=[CH:15][CH:14]=2)[C:8](=[O:21])[CH2:7]1)(=[O:5])=[O:4].[Cl:22][C:23]1[CH:30]=[C:27]([CH:28]=O)[C:26]([OH:31])=[CH:25][CH:24]=1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+]>CN(C=O)C>[Cl:22][C:23]1[CH:24]=[CH:25][C:26]2[O:31][C:2]([S:3]([N:6]3[CH2:11][CH2:10][N:9]([CH2:12][C:13]4[CH:18]=[CH:17][C:16]([C:19]#[N:20])=[CH:15][CH:14]=4)[C:8](=[O:21])[CH2:7]3)(=[O:5])=[O:4])=[CH:28][C:27]=2[CH:30]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 4875Potassium IodideHCID 11430Potassium CarbonateHCID 124815-Chloro-salicylaldehydeHCID 23447429HCID 23447429, 화합물

생성물 1

HCID 23447401HCID 23447401, 화합물수율 9.2%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

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온도
80 °C

실험 절차

A mixture of 4-chloromethylsulfonyl-1-(4-cyanobenzyl)-2-piperazinone (3.20 g), 5-chlorosalicylaldehyde (2.29 g), potassium carbonate (1.48 g), potassium iodide (1.62 g) and DMF (80 ml) was stirred at 80° C. for 2 days. The reaction solution was concentrated under reduced pressure, and to the residue was added ethyl acetate. The mixture was washed with water and saturated brine, dried (MgSO4) and concentrated, and the residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1) to give colorless crystals of the title compound (384 mg).

후처리

  1. concentrationThe reaction solution was concentrated under reduced pressure
  2. additionto the residue was added ethyl acetate
  3. washThe mixture was washed with water and saturated brine
  4. dry with materialdried (MgSO4)
  5. concentrationconcentrated
  6. customthe residue was purified with silica gel column chromatography (hexane:ethyl acetate=1:1)

출처 및 근거

ORD 기록
ord-a53100f67777487dbdf667161bf932bc
출처 데이터셋
uspto-grants-2002_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06403595B1

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