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

HRID 626522
ノート
印刷プレビュー

反応式

HRID 626522 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 2

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

生成物 1

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

試薬・触媒・溶媒 4

HCID 23994Zinc触媒HCID 887Methanol溶媒
HCID 8028
Tetrahydrofuran
溶媒
HCID 8857Ethyl Acetate溶媒

実験手順

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+).

後処理

  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

出典と根拠

ORDレコード
ord-8043326d56624ce383c966b7357af6c7
出典データセット
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09309224B2

反応ノート

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