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Iodine → Adenosine antagonist-1

HRID 2214766
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HRID 2214766 반응식
[CH3:1][C:2]1[N:3]([CH2:7][C:8]([C:10]2[CH:11]=[C:12]([CH:15]=[CH:16][CH:17]=2)[C:13]#[N:14])=O)[CH:4]=[CH:5][N:6]=1.[N:18]1[CH:23]=[CH:22][N:21]=[CH:20][C:19]=1[NH:24][C:25]([NH2:27])=[S:26].II.N1C=CC=CC=1>O>[CH3:1][C:2]1[N:3]([C:7]2[S:26][C:25]([NH:24][C:19]3[CH:20]=[N:21][CH:22]=[CH:23][N:18]=3)=[N:27][C:8]=2[C:10]2[CH:11]=[C:12]([CH:15]=[CH:16][CH:17]=2)[C:13]#[N:14])[CH:4]=[CH:5][N:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 807IodineHCID 1049PyridineHCID 2771013N-PyrazinylthioureaHCID 219484043-(2-(2-Methyl-1H-imidazol-1-YL)acetyl)benzonitrile

생성물 1

HCID 10291948Adenosine antagonist-1

시약·촉매·용매 1

HCID 962Water용매

실험 절차

3-(2-Methylimidazol-1-yl-acetyl)-benzonitrile (13.8 g, 0.06 mol) is mixed with pyrazinyl-2-thiourea (9.4 g, 0.06 mol), iodine (15.6 g, 0.06 mol) and pyridine (60 ml). The mixture is stirred, initially at room temperature and then at 60° C. overnight (17.5 hours). The mixture obtained is allowed to cool to room temperature and water (50 ml) added. The solid obtained is filtered off, stirred in water (50 ml) for 30 minutes, and filtered off again. The resulting solid is dried at 40° C. in vacuo over P2O5 to give the title compound.

후처리

  1. customat 60° C.
  2. customovernight (17.5 hours)
  3. customThe mixture obtained
  4. temperatureto cool to room temperature
  5. customThe solid obtained
  6. filtrationis filtered off
  7. stirringstirred in water (50 ml) for 30 minutes
  8. filtrationfiltered off again
  9. dry with materialThe resulting solid is dried at 40° C. in vacuo over P2O5

출처 및 근거

ORD 기록
ord-17dd3010644f45378a24ef7adaa44eb5
출처 데이터셋
uspto-grants-2006_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07109202B2

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