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1,8-Diazabicyclo(5.4.0)undec-7-ene → 7-Chloro-2-(2-furyl)-5-methylthio[1,2,4]triazolo[1,5-c]pyrimidine

HRID 1264870
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HRID 1264870 반응식
[Cl:1][C:2]1[N:7]=[C:6]([S:8][CH3:9])[N:5]2[C:10]([C:13]3[O:14][CH:15]=[CH:16][CH:17]=3)=[N:11][N:12]=[C:4]2[CH:3]=1.C1CCN2C(=NCCC2)CC1>C1COCC1>[Cl:1][C:2]1[N:7]=[C:6]([S:8][CH3:9])[N:12]2[N:11]=[C:10]([C:13]3[O:14][CH:15]=[CH:16][CH:17]=3)[N:5]=[C:4]2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 186137007-Chloro-3-(furan-2-yl)-5-(methylsulfanyl)[1,2,4]triazolo[4,3-c]pyrimidine

생성물 1

HCID 186136967-Chloro-2-(2-furyl)-5-methylthio[1,2,4]triazolo[1,5-c]pyrimidine수율 81%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Into 8.5 mL of THF, 2.7 g (10 mmol) of Compound B was dissolved, and 1.5 mL (10 mmol) of DBU was added thereto under ice cooling, followed by stirring at room temperature for about 1 hour. During the period, crystals were precipitated from the reaction solution. After completion of the reaction, the precipitated solid was washed with THF to obtain 2.1 g of Compound C as a white solid (yield: 81%).

후처리

  1. customDuring the period, crystals were precipitated from the reaction solution
  2. customAfter completion of the reaction
  3. washthe precipitated solid was washed with THF

출처 및 근거

ORD 기록
ord-6506748aabe44da5af3a52bdf9c0354b
출처 데이터셋
uspto-grants-2003_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06545000B1

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