反応式
[CH3:1][O:2][C:3]([C:5]1[C:10](Cl)=[N:9][CH:8]=[CH:7][N:6]=1)=[O:4].O.[SH-:13].[Na+]>CO>[CH3:1][O:2][C:3]([C:5]1[C:10]([SH:13])=[N:9][CH:8]=[CH:7][N:6]=1)=[O:4]参加物
4
実験手順
After 3-chloro-pyrazine-2-carboxylic acid methyl ester (0.4 g, 2.3 mmol) was dissolved in MeOH (46 mL), sodium hydrosulfide monohydrate (0.65 g, 6.9 mmol) was added thereto, and the mixture was stirred at room temperature for 9 hours. After the termination of the reaction, the reactant was concentrated under reduced pressure, and 1N HCl aqueous solution was used to adjust the pH of the reactant to 3. The reactant was extracted with EtOAc, and the organic layer was separated to obtain the title compound (0.35 g, 89%).
後処理
- customAfter the termination of the reaction
- concentrationthe reactant was concentrated under reduced pressure, and 1N HCl aqueous solution
- extractionThe reactant was extracted with EtOAc
- customthe organic layer was separated
出典と根拠
- ORDレコード
- ord-f1f4215d401d4b258248d4ffd75b3f69
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09447044B2
関連ノート
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