Pyridine, hydrofluoride (1:1) → (4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone

反応式

[F:1][C:2]([CH3:9])([CH3:8])[CH2:3][C@@H:4]([CH2:6][OH:7])[NH2:5].CC(=C)C[C@H]1C[O:16][C:15](=O)N1.C1C=CN=CC=1.F>>[F:1][C:2]([CH3:9])([CH3:8])[CH2:3][C@H:4]1[CH2:6][O:7][C:15](=[O:16])[NH:5]1

参加物

反応物 3

HCID 64774Pyridine, hydrofluoride (1:1)

HCID 12167160(2S)-2-amino-4-fluoro-4-methylpentan-1-ol

HCID 57463978(4S)-4-(2-methylprop-2-enyl)-1,3-oxazolidin-2-one

生成物 1

HCID 11194496(4S)-4-(2-Fluoro-2-methylpropyl)-2-oxazolidinone

実験手順

The 4-fluoroleucinol can also be synthesized according to Scheme 8. 4,5-Dehydroleucine is converted to (4S)-4-(2-methylprop-2-enyl)-1,3-oxazolidin-2-one as described in the scheme below. This intermediate is then treated with a hydrofluorination reagent such as HF-pyridine to give (4S)-4-(2-fluoro-2-methylpropyl)-1,3-oxazolidin-2-one. Basic hydrolysis (i.e. Ba(OH)2 or NaOH) then affords (2S)-2-amino-4-fluoro-4-methylpentan-1-ol.

出典と根拠

ORDレコード: ord-c925986e65fa4f97b789cedbfae3df4f
出典データセット: uspto-grants-2014_07
DOI: 10.6084/m9.figshare.5104873.v1
特許番号: US08772336B2

反応ノート

読み込み中…

参加物