2,4-Dichloropyridine → 4-(2-Chloro-pyridin-4-yloxy)-2,3-difluorophenylamine

反応式

[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([OH:8])=[C:4]([F:9])[C:3]=1[F:10].CC(C)([O-])C.[K+].[Cl:17][C:18]1[CH:23]=[C:22](Cl)[CH:21]=[CH:20][N:19]=1>>[Cl:17][C:18]1[CH:23]=[C:22]([O:8][C:5]2[CH:6]=[CH:7][C:2]([NH2:1])=[C:3]([F:10])[C:4]=2[F:9])[CH:21]=[CH:20][N:19]=1

参加物

反応物 3

HCID 335152,4-Dichloropyridine

HCID 27787664-Amino-2,3-difluorophenol

HCID 23665647Potassium tert-butoxide

生成物 1

HCID 866238534-(2-Chloro-pyridin-4-yloxy)-2,3-difluorophenylamine収率 66%

実験手順

Using a procedure analogous to Example A2, 4-amino-2,3-difluorophenol (6 g, 41.4 mmol), potassium tert-butoxide (4.9 g, 43.5 mmol) and 2,4-dichoropyridine (6.1 g, 41.4 mmol) were combined to afford 4-(2-chloro-pyridin-4-yloxy)-2,3-difluorophenylamine (7 g, 66% yield). 1H NMR (400 MHz, DMSO-d6) δ 8.27 (d, J=6.0 Hz, 1H), 7.05 (s, 1H), 6.95 (m, 1H), 6.92 (d, J=8.8 Hz, 1H), 6.62 (d, J=8.8 Hz, 1H), 5.60 (s, 2H).

出典と根拠

ORDレコード: ord-b46eb5177a114c3b9cf17345ee0d167f
出典データセット: uspto-grants-2010_09
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US07790756B2

反応ノート

読み込み中…

参加物