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Diethyl Ether → HCID 178503523, 화합물

HRID 1027485
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HRID 1027485 반응식
[OH:1][C:2]1[C:7]([NH:8][C:9](=[O:17])[C:10]2[CH:15]=[CH:14][CH:13]=[C:12]([CH3:16])[CH:11]=2)=[C:6](O)[N:5]=[C:4]([S:19][CH3:20])[N:3]=1.C(OCC)C>P(Cl)(Cl)(Cl)=O>[CH3:20][S:19][C:4]1[N:3]=[C:2]([OH:1])[C:7]2[N:8]=[C:9]([C:10]3[CH:15]=[CH:14][CH:13]=[C:12]([CH3:16])[CH:11]=3)[O:17][C:6]=2[N:5]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 3283Diethyl EtherHCID 178503566HCID 178503566, 화합물

생성물 1

HCID 178503523HCID 178503523, 화합물수율 38.6%

시약·촉매·용매 1

HCID 24813Phosphorus oxychloride용매

실험 절차

21 g of N-(4,6-dihydroxy-2-methylsulfanyl-pyrimidin-5-yl)-3-methyl-benzamide in 100 ml of phosphorus oxychloride were heated to 70° C. for 3 h. After cooling, the mixture was poured into 500 ml of diethyl ether. The precipitate was filtered off and washed with diethyl ether. 7.6 g of the title compound were obtained.

후처리

  1. temperatureAfter cooling
  2. filtrationThe precipitate was filtered off
  3. washwashed with diethyl ether

출처 및 근거

ORD 기록
ord-7623b55efad844c793a76286241d0ccb
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08735387B2

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