Bromopyruvic Acid → 2-(Isopropylamino)thiazole-4-carboxylic acid hydrobromide
反応式
[CH:1]([NH:4][C:5]([NH2:7])=[S:6])([CH3:3])[CH3:2].[Br:8][CH2:9][C:10](=O)[C:11]([OH:13])=[O:12]>O1CCOCC1>[BrH:8].[CH:1]([NH:4][C:5]1[S:6][CH:9]=[C:10]([C:11]([OH:13])=[O:12])[N:7]=1)([CH3:3])[CH3:2]参加物
4
反応条件
- 温度
- 80 °C
実験手順
A suspension of compound 9 (2.1 g, 18 mmol) and 3-bromopyruvic acid (3.0 g, 18 mmol) in dioxane (180 mL) was heated to 80° C. Upon reaching 80° C. the mixture became clear, and soon thereafter the product started to precipitate as a white solid. After 2 h of heating, the reaction mixture was cooled to rt and the precipitate was filtered off and collected. This yielded pure title compound (4.4 g, 94%).
後処理
- customUpon reaching 80° C.
- customto precipitate as a white solid
- temperatureAfter 2 h of heating
- temperaturethe reaction mixture was cooled to rt
- filtrationthe precipitate was filtered off
- customcollected
出典と根拠
- ORDレコード
- ord-3ba9ce36669844d78c4a8f5bac9e6f5e
- 出典データセット
- uspto-grants-2010_04
- 特許番号
- US07700552B2
反応ノート
読み込み中…