Propargylamine → 6-Chloro-5-(2-propyn-1-ylamino)-2-pyrazinecarboxylic acid
反応式
Cl[C:2]1[C:7]([Cl:8])=[N:6][C:5]([C:9]([OH:11])=[O:10])=[CH:4][N:3]=1.[NH2:12][CH2:13][C:14]#[CH:15]>O1CCOCC1>[Cl:8][C:7]1[C:2]([NH:12][CH2:13][C:14]#[CH:15])=[N:3][CH:4]=[C:5]([C:9]([OH:11])=[O:10])[N:6]=1参加物
4
実験手順
A mixture of 2,3-dichloropyrazine-5-carboxylic acid (19.3 g, 0.100 mole) and 3-amino-1-propyne (1.10 g, 0.20 mole) in 100 ml dioxane is refluxed for 24 hours, cooled and concentrated under vacuum. The residue is partitioned between aqueous sodium bicarbonate and chloroform and the aqueous extract neutralized with acetic acid to give a precipitate of 3-chloro-2-(2-propyn-1-ylamino)pyrazine-5-carboxylic acid.
後処理
- temperatureis refluxed for 24 hours
- temperaturecooled
- concentrationconcentrated under vacuum
- customThe residue is partitioned between aqueous sodium bicarbonate and chloroform
- extractionthe aqueous extract
出典と根拠
- ORDレコード
- ord-21e9929954bc4d0b8f2691a5f480b50c
- 出典データセット
- uspto-grants-1980_12
- 特許番号
- US04242344
反応ノート
読み込み中…