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(4,6-Dibromopyrimidin-2-yl)-methylamine → [4-Bromo-6-(4-nitrophenylsulphanyl)-pyrimidin-2-yl]-methylamine

HRID 1603546
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HRID 1603546 반응식
Br[C:2]1[CH:7]=[C:6]([Br:8])[N:5]=[C:4]([NH:9][CH3:10])[N:3]=1.[K].[N+:12]([C:15]1[CH:20]=[CH:19][C:18]([SH:21])=[CH:17][CH:16]=1)([O-:14])=[O:13]>CN1CCCC1=O>[Br:8][C:6]1[CH:7]=[C:2]([S:21][C:18]2[CH:19]=[CH:20][C:15]([N+:12]([O-:14])=[O:13])=[CH:16][CH:17]=2)[N:3]=[C:4]([NH:9][CH3:10])[N:5]=1
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참가 물질

4

반응물 2

HCID 19605496(4,6-Dibromopyrimidin-2-yl)-methylamineHCID 700026814Nitrothiophenol potassium salt

생성물 1

HCID 19605548[4-Bromo-6-(4-nitrophenylsulphanyl)-pyrimidin-2-yl]-methylamine수율 56.4%

시약·촉매·용매 1

HCID 13387N-methyl-2-pyrrolidone용매

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온도
50 °C

실험 절차

0.70 g (0.0026 mol) of (4,6-dibromopyrimidin-2-yl)-methylamine and 0.56 g (0.0026 mol) of 4-nitrothiophenol potassium salt were dissolved in 15 ml of 1-methyl-2-pyrrolidone and stirred at 50° C. for 5 hrs. The solvent was removed and the residue was partitioned in water and ethyl acetate. The combined organic phases were washed with sat. sodium chloride solution and dried over MgSO4. After filtration and removal of the solvent the residue was chromatographed on silica gel with ethyl acetate/hexane 1:9 and subsequently dried in a high vacuum. There was obtained 0.50 g (56%) of [4-bromo-6-(4-nitrophenylsulphanyl)-pyrimidin-2-yl]-methylamine as yellow crystals; m.p.: 204-205° C.

후처리

  1. customThe solvent was removed
  2. customthe residue was partitioned in water
  3. washThe combined organic phases were washed with sat. sodium chloride solution
  4. dry with materialdried over MgSO4
  5. filtrationAfter filtration and removal of the solvent the residue
  6. customwas chromatographed on silica gel with ethyl acetate/hexane 1:9
  7. customsubsequently dried in a high vacuum

출처 및 근거

ORD 기록
ord-3cd8662efec04839942344a00aa271a1
출처 데이터셋
uspto-grants-1999_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05990105

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