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2,5-Dichloro-4-(6-fluoropyridin-2-yl)pyrimidine → HCID 178511659, 화합물

HRID 1963853
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HRID 1963853 반응식
Cl[C:2]1[N:7]=[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[N:9]=2)[C:5]([Cl:15])=[CH:4][N:3]=1.[C@H:16]1([NH2:23])[CH2:21][CH2:20][C@H:19]([NH2:22])[CH2:18][CH2:17]1>CS(C)=O>[Cl:15][C:5]1[C:6]([C:8]2[CH:13]=[CH:12][CH:11]=[C:10]([F:14])[N:9]=2)=[N:7][C:2]([NH:22][C@H:19]2[CH2:20][CH2:21][C@H:16]([NH2:23])[CH2:17][CH2:18]2)=[N:3][CH:4]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 866506062,5-Dichloro-4-(6-fluoropyridin-2-yl)pyrimidineHCID 178511674HCID 178511674, 화합물

생성물 1

HCID 178511659HCID 178511659, 화합물수율 80.8%

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매

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온도
75 °C

실험 절차

A mixture of 2,5-dichloro-4-(6-fluoropyridin-2-yl)pyrimidine (37 mg, 0.152 mmol), DMSO (1.5 ml) and trans-cyclohexane-1,4-diamine (87 mg, 0.758 mmol)reaction mixture was stirred at about 75° C. for about 2 hours. The reaction mixture was cooled, filter and purified by prep LC, and then lyophilized to yield 39.5 mg of the title compound as a TFA salt. LCMS (m/z): 322.2 (MH+), retention time=0.59 min.

후처리

  1. temperatureThe reaction mixture was cooled
  2. filtrationfilter
  3. custompurified by prep LC

출처 및 근거

ORD 기록
ord-fa28fef590ab4fd191574e7e81110101
출처 데이터셋
uspto-grants-2013_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08415381B2

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