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Dichloromethane → 2-(4-(6-Chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanol

HRID 515245
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HRID 515245 반응식
[OH:1][CH2:2][CH2:3][N:4]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1.[CH3:10][C:11]1[N:16]=[C:15](Cl)[CH:14]=[C:13]([Cl:18])[N:12]=1.C(Cl)Cl>C(N(CC)CC)C>[Cl:18][C:13]1[N:12]=[C:11]([CH3:10])[N:16]=[C:15]([N:7]2[CH2:8][CH2:9][N:4]([CH2:3][CH2:2][OH:1])[CH2:5][CH2:6]2)[CH:14]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 6344DichloromethaneHCID 76771-(2-Hydroxyethyl)piperazine2회HCID 2349974,6-Dichloro-2-methylpyrimidine2회

생성물 1

HCID 144795582-(4-(6-Chloro-2-methylpyrimidin-4-yl)piperazin-1-yl)ethanol수율 89.8%

시약·촉매·용매 1

HCID 8471Triethylamine용매

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온도
30 °C

실험 절차

1-(2-hydroxyethyl)piperazine (Compound 3) (16.6 g, 127.6 mmol)) and 2-methyl-4,6-dichloropyrimidine (Compound 2) (10.4 g, 63.8 mmol) were mixed with methylene dichloride (80 mL) in reaction flask to be stirred for 2.5 h at 30° C., and then triethylamine (1.8 mL) was added with the reaction overnight in thermal insulation. After vacuum filtration, the cake was rinsed by methylene dichloride. The filtrate was vacuum condensed to dry, and then n-hexane (40 mL) was added to grow the grains for 1 h by stirring. After vacuum filtration, the cake was rinsed by n-hexane (20 mL) and dried at 40° C. to constant weight to give white solid target Compound 4 (14.7 g, yield: 89.8%).

후처리

  1. filtrationAfter vacuum filtration
  2. washthe cake was rinsed by methylene dichloride
  3. customvacuum condensed
  4. customto dry
  5. additionn-hexane (40 mL) was added
  6. customfor 1 h
  7. stirringby stirring
  8. filtrationAfter vacuum filtration
  9. washthe cake was rinsed by n-hexane (20 mL)
  10. customdried at 40° C. to constant weight

출처 및 근거

ORD 기록
ord-9c2895924dc74897ab2ed8b4c70ac49f
출처 데이터셋
uspto-grants-2015_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09108954B2

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