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3,6-Dichloropyridazine → 3-[4-(6-Chloropyridazin-3-yl)piperazin-1-yl]propane-1,2-diol

HRID 231763
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HRID 231763 반응식
[OH:1][CH:2]([CH2:10][OH:11])[CH2:3][N:4]1[CH2:9][CH2:8][NH:7][CH2:6][CH2:5]1.[Cl:12][C:13]1[N:14]=[N:15][C:16](Cl)=[CH:17][CH:18]=1>C(O)(C)C>[Cl:12][C:13]1[N:14]=[N:15][C:16]([N:7]2[CH2:8][CH2:9][N:4]([CH2:3][CH:2]([OH:1])[CH2:10][OH:11])[CH2:5][CH2:6]2)=[CH:17][CH:18]=1
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참가 물질

4

반응물 2

HCID 673313,6-DichloropyridazineHCID 1110023-(Piperazin-1-yl)propane-1,2-diol

생성물 1

HCID 200320123-[4-(6-Chloropyridazin-3-yl)piperazin-1-yl]propane-1,2-diol

시약·촉매·용매 1

HCID 3776Isopropanol용매

실험 절차

Grams 32 of 1-(2,3-dihydroxypropyl)piperazine and 15 g of 3,6-dichloropyridazine in 700 ml isopropanol were refluxed for 24 hours. The reaction mixture was settled, the solid undissolvable removed and the solution evaporated to dryness. The so obtained residue was purified on column eluting with chloroform:methanol (9:1). Grams 2.1 of 3-[4-(6-chloropyridazin-3-yl)piperazin-1-yl]propane-1,2-diol, which, recrystallized from acetone, melted at 126°-128° C.

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후처리

  1. customthe solid undissolvable removed
  2. customthe solution evaporated to dryness
  3. customThe so obtained residue
  4. customwas purified on column
  5. washeluting with chloroform:methanol (9:1)
  6. customGrams 2.1 of 3-[4-(6-chloropyridazin-3-yl)piperazin-1-yl]propane-1,2-diol, which, recrystallized from acetone, melted at 126°-128° C.

출처 및 근거

ORD 기록
ord-09a899ee5eb7470b9150cd42a19f1862
출처 데이터셋
uspto-grants-1989_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04849422

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