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Ammonium Chloride → 3-(4-((6-Amino-2-methylpyridin-3-yl)oxy)pyridin-2-yl)-1,1-dimethylurea

HRID 626522
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HRID 626522 반응식
[CH3:1][N:2]([CH3:23])[C:3]([NH:5][C:6]1[CH:11]=[C:10]([O:12][C:13]2[C:14]([CH3:22])=[N:15][C:16]([N+:19]([O-])=O)=[CH:17][CH:18]=2)[CH:9]=[CH:8][N:7]=1)=[O:4].[NH4+].[Cl-]>CO.C1COCC1.CCOC(C)=O.[Zn]>[NH2:19][C:16]1[N:15]=[C:14]([CH3:22])[C:13]([O:12][C:10]2[CH:9]=[CH:8][N:7]=[C:6]([NH:5][C:3](=[O:4])[N:2]([CH3:23])[CH3:1])[CH:11]=2)=[CH:18][CH:17]=1
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참가 물질

7

반응물 2

HCID 25517Ammonium ChlorideHCID 904098671,1-Dimethyl-3-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)urea

생성물 1

HCID 904098553-(4-((6-Amino-2-methylpyridin-3-yl)oxy)pyridin-2-yl)-1,1-dimethylurea수율 113%

시약·촉매·용매 4

HCID 23994Zinc촉매HCID 887Methanol용매
HCID 8028
Tetrahydrofuran
용매
HCID 8857Ethyl Acetate용매

실험 절차

A mixture of 1,1-dimethyl-3-(4-((2-methyl-6-nitropyridin-3-yl)oxy)pyridin-2-yl)urea (0.500 g, 1.576 mmol) and NH4Cl (2.53 g, 47.3 mmol) in MeOH (10 mL) and THF (10 mL) was treated with zinc dust (1.030 g, 15.76 mmol) and stirred at RT for 0.5 h. The mixture was diluted with EtOAc, the solids removed via filtration, washed with EtOAc and the filtrate concentrated to dryness. The residue was treated with DCM, sonicated, the solids removed via filtration and the filtrate concentrated to dryness to afford 3-(4-((6-amino-2-methylpyridin-3-yl)oxy)pyridin-2-yl)-1,1-dimethylurea (510 mg, 113%). MS (ESI) m/z: 288.1 (M+H+).

후처리

  1. customthe solids removed via filtration
  2. washwashed with EtOAc
  3. concentrationthe filtrate concentrated to dryness
  4. additionThe residue was treated with DCM
  5. customsonicated
  6. customthe solids removed via filtration
  7. concentrationthe filtrate concentrated to dryness

출처 및 근거

ORD 기록
ord-8043326d56624ce383c966b7357af6c7
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309224B2

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