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Ammonium Chloride → 3-Fluoro-4-(pyrrolo[2,1-f][1,2,4]triazin-4-yloxy)benzenamine

HRID 2117079
ノート
印刷プレビュー

反応式

HRID 2117079 の反応式
[F:1][C:2]1[CH:17]=[C:16]([N+:18]([O-])=O)[CH:15]=[CH:14][C:3]=1[O:4][C:5]1[C:10]2=[CH:11][CH:12]=[CH:13][N:9]2[N:8]=[CH:7][N:6]=1.[Cl-].[NH4+]>O1CCCC1.CO.[Zn]>[F:1][C:2]1[CH:17]=[C:16]([NH2:18])[CH:15]=[CH:14][C:3]=1[O:4][C:5]1[C:10]2=[CH:11][CH:12]=[CH:13][N:9]2[N:8]=[CH:7][N:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 2

HCID 25517Ammonium Chloride2 回HCID 210816564-(2-Fluoro-4-nitrophenoxy)pyrrolo[2,1-f][1,2,4]triazine

生成物 1

HCID 210816213-Fluoro-4-(pyrrolo[2,1-f][1,2,4]triazin-4-yloxy)benzenamine収率 92.5%

試薬・触媒・溶媒 3

HCID 23994Zinc触媒2 回HCID 887Methanol溶媒
HCID 8028
Tetrahydrofuran
溶媒

実験手順

To a solution of 4-(2-fluoro-4-nitrophenoxy)pyrrolo[2,1-f][1,2,4]triazine (4.25 g, 15.5 mmol) in 40 mL of tetrahydrofuran and 60 mL of methanol at 0° C. was added zinc dust (3.04 g, 46.5 mmol, <10 micron) followed by ammonium chloride (2.49 g, 46.5 mmol). The mixture was stirred at room temperature overnight. Additional zinc dust (6.08 g, 93 mmol) and ammonium chloride (5.0 g, 93 mmol) were added and the reaction was allowed to stir at room temperature for 4 h. The heterogeneous mixture was filtered through a thin pad of Celite® with methanol and the filtrate was concentrated in vacuo. Purification by flash chromatography on silica gel (SiO2, EtOAc/Hexane 1:1) gave the title compound (3.5 g, 92%) as a yellow foam.

後処理

  1. stirringto stir at room temperature for 4 h
  2. filtrationThe heterogeneous mixture was filtered through a thin pad of Celite® with methanol
  3. concentrationthe filtrate was concentrated in vacuo
  4. customPurification by flash chromatography on silica gel (SiO2, EtOAc/Hexane 1:1)

出典と根拠

ORDレコード
ord-98b0392fc7c54bcc88ebc4fc8e06a41a
出典データセット
uspto-grants-2008_10
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07439246B2

反応ノート

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