Acetic Anhydride → 4-((5-Fluoropyridin-2-yl)methoxy)pyridin-2(1H)-one

HRID 882021

反応式

HRID 882021 の反応式
[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][O:9][C:10]2[CH:15]=[CH:14][N+:13]([O-])=[CH:12][CH:11]=2)=[N:6][CH:7]=1.C(OC(=O)C)(=[O:19])C>>[F:1][C:2]1[CH:3]=[CH:4][C:5]([CH2:8][O:9][C:10]2[CH:15]=[CH:14][NH:13][C:12](=[O:19])[CH:11]=2)=[N:6][CH:7]=1

参加物

3

反応条件

温度
80 °C

実験手順

4-((5-Fluoropyridin-2-yl)methoxy)pyridine 1-oxide (1.76 g, 7.99 mmol) was heated to 140° C. in acetic anhydride (80 mL) for 5 h. The mixture was concentrated and then heated at 80° C. for 1 h in a mixture of MeOH (20 mL) and aqueous 1 N NaOH (15 mL). The resulting black solution was concentrated to a volume of 15 mL, and the solid was filtered off, rinsed with CH2Cl2 and dried under vacuum to provide the title compound (1.29 g, 73%) as a yellow solid: 1H NMR (500 MHz, DMSO-d6) δ 11.12 (s, 1H), 8.59 (d, J=2.9 Hz, 1H), 7.79 (ddd, J=8.7, 8.7, 2.9 Hz, 1H), 7.60 (dd, J=8.7, 4.5 Hz, 1H), 7.26 (d, J=7.3 Hz, 1H), 5.95 (dd, J=7.4, 2.6 Hz, 1H), 5.78 (d, J=2.5 Hz, 1H), 5.12 (s, 2H).

後処理

  1. concentrationThe mixture was concentrated
  2. concentrationThe resulting black solution was concentrated to a volume of 15 mL
  3. filtrationthe solid was filtered off
  4. washrinsed with CH2Cl2
  5. customdried under vacuum

出典と根拠

ORDレコード
ord-06a02b8338c3446395b158e4b8143ca7
出典データセット
uspto-grants-2015_03
特許番号
US08993765B2

関連ノート

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