Sodium borohydride → HCID 11047852、化合物
反応式
[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[F:19])[N:15]=[C:14]([I:20])[C:13]([CH:21]=[O:22])=[CH:12]2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[BH4-].[Na+]>CO>[CH2:1]([O:8][C:9]1[CH:10]=[C:11]2[C:16](=[CH:17][C:18]=1[F:19])[N:15]=[C:14]([I:20])[C:13]([CH2:21][OH:22])=[CH:12]2)[C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1参加物
4
実験手順
A suspension of 6-benzyloxy-7-fluoro-2-iodo-3-quinolinecarbaldehyde (obtained according to 1.e, 13 g, 32 mmol) in methanol (100 ml) is treated with sodium borohydride (1.85 g, 48 mmol). After 1 hour of reaction, the reaction medium is concentrated under reduced pressure then taken up with water, filtered, washed with water and ethanol in order to produce, after drying under reduced pressure, 10 g (76%) of a white solid, m.p. 188° C.
後処理
- customAfter 1 hour of reaction
- concentrationthe reaction medium is concentrated under reduced pressure
- filtrationfiltered
- washwashed with water and ethanol in order
- customto produce
- dry with materialafter drying under reduced pressure, 10 g (76%) of a white solid, m.p. 188° C.
出典と根拠
- ORDレコード
- ord-ea7d5449aba440ba9a6ce7d826699629
- 出典データセット
- uspto-grants-2002_08
- 特許番号
- US06436951B1
反応ノート
読み込み中…