Hydrochloric Acid → 3-Amino-5,6-bis(trifluoromethyl)pyrazine-2-carbohydrazide
反応式
[NH2:1][C:2]1[C:3]([C:16](OCC)=[O:17])=[N:4][C:5]([C:12]([F:15])([F:14])[F:13])=[C:6]([C:8]([F:11])([F:10])[F:9])[N:7]=1.O.[NH2:22][NH2:23].Cl>CO.O>[NH2:1][C:2]1[C:3]([C:16]([NH:22][NH2:23])=[O:17])=[N:4][C:5]([C:12]([F:14])([F:15])[F:13])=[C:6]([C:8]([F:11])([F:10])[F:9])[N:7]=1参加物
6
実験手順
A suspension of ethyl 3-amino-5,6-bis(trifluoromethyl)pyrazine-2-carboxylate (Int. G1)(455 mg, 1.501 mmol) in MeOH (10 ml) was treated with hydrazine monohydrate (0.147 ml, 3.00 mmol) and stirred at RT overnight. The reaction mixture was diluted with water (50 ml) and the pH was adjusted to pH4-5 using 1M HCl. A yellow precipitate formed which was filtered under vacuum, washed with water and air dried to afford the title compound which was used without further purification;
後処理
- customA yellow precipitate formed which
- filtrationwas filtered under vacuum
- washwashed with water and air
- customdried
出典と根拠
- ORDレコード
- ord-4b9721b5aba7433ebc7a754459f50caa
- 出典データセット
- uspto-grants-2015_05
- 特許番号
- US09034879B2
反応ノート
読み込み中…