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HCID 24902159, 화합물 → HCID 25132978, 화합물

HRID 1890980
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인쇄 미리보기

반응식

HRID 1890980 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH2:8][S:9]([NH-:12])(=[O:11])=[O:10])[CH:5]=[CH:6][CH:7]=1.Cl[C:14]1[CH:19]=[C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=2[CH2:26][CH3:27])[N:17]=[CH:16][N:15]=1>CN(C=O)C>[CH2:26]([C:21]1[CH:22]=[CH:23][CH:24]=[CH:25][C:20]=1[C:18]1[N:17]=[CH:16][N:15]=[C:14]([NH:1][C:2]2[CH:3]=[C:4]([CH2:8][S:9]([NH2:12])(=[O:10])=[O:11])[CH:5]=[CH:6][CH:7]=2)[CH:19]=1)[CH3:27]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 24902159HCID 24902159, 화합물HCID 86660187HCID 86660187, 화합물

생성물 1

HCID 25132978HCID 25132978, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
80 °C

실험 절차

A mixture of (3-aminophenyl)methanesulfonyl amide (0.112 g, 0.60 mmol) and 4-chloro-6-(2-ethylphenyl)-pyrimidine (0.131 g, 0.60 mmol) in DMFA (3 mL) was stirred at 80° C. till the reaction completion (TLC control), then concentrated in vacuo, and the residue was recrystallized from isopropanol to give {3-[6-(2-ethyl-phenyl)-pyrimidin-4-ylamino]-phenyl}-methanesulfonamide (Compound 26)

후처리

  1. concentrationconcentrated in vacuo
  2. customthe residue was recrystallized from isopropanol

출처 및 근거

ORD 기록
ord-21ce72215db3430c857d49097a5cc5b9
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08507498B2

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