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Potassium Carbonate → 3-Amino-6-[(3-propylimidazol-4-yl)methylthio]pyridazine

HRID 856628
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인쇄 미리보기

반응식

HRID 856628 반응식
[NH2:1][C:2]1[N:3]=[N:4][C:5]([SH:8])=[CH:6][CH:7]=1.Cl.Cl[CH2:11][C:12]1[N:13]([CH2:17][CH2:18][CH3:19])[CH:14]=[N:15][CH:16]=1.C(=O)([O-])[O-].[K+].[K+]>CN(C)C=O>[NH2:1][C:2]1[N:3]=[N:4][C:5]([S:8][CH2:11][C:12]2[N:13]([CH2:17][CH2:18][CH3:19])[CH:14]=[N:15][CH:16]=2)=[CH:6][CH:7]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 229386165-(chloromethyl)-1-propyl-1H-imidazole hydrochlorideHCID 178507803CID 79851

생성물 1

HCID 695227193-Amino-6-[(3-propylimidazol-4-yl)methylthio]pyridazine수율 65.6%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

3-amino-6-mercaptopyridazine (0.5 g), 4-chloromethyl-3-propylimidazole hydrochloride (0.62 g) and potassium carbonate (2.0 g) were added to N,N-dimethylformamide (10 ml), and the mixture was stirred overnight at room temperature. The solvent was distilled off, the residue was purified by basic silica gel column chromatography (elution solvent: methanol/ethyl acetate), to give 3-amino-6-[(3-propylimidazol-4-yl)methylthio]pyridazine (0.52 g) as yellow crystals.

후처리

  1. distillationThe solvent was distilled off
  2. customthe residue was purified by basic silica gel column chromatography (elution solvent: methanol/ethyl acetate)

출처 및 근거

ORD 기록
ord-326aa6da01b9404dbd49eeb93e9415a8
출처 데이터셋
uspto-grants-2007_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07262185B2

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