反応式
[NH2:1][NH2:2].[Cl:3][C:4]1[CH:9]=[C:8](Cl)[N:7]=[C:6]([S:11][CH3:12])[N:5]=1>ClCCl>[Cl:3][C:4]1[N:5]=[C:6]([S:11][CH3:12])[N:7]=[C:8]([NH:1][NH2:2])[CH:9]=1参加物
4
反応条件
- 温度
- -78 °C
実験手順
Referring to Scheme 2, anhydrous hydrazine (164 mg, 162 μl, 5.1 mmol) and dichloromethane (3 ml) were cooled to −78° C. 4,6-Dichloro-2-(methylthio)pyrimidine (1 g, 5.1 mmol) was slowly added. The mixture was allowed to stir for 10 minutes then the bath was replaced with an ice bath and the solution allowed to slowly reach 0° C. The precipitate was filtered and washed with DCM. 1-(6-Chloro-2-(methylthio)pyrimidin-4-yl)hydrazine (624 mg, 64%) was obtained. [M+H] calc'd for C5H7ClN4S, 191; found, 191.
後処理
- customthe bath was replaced with an ice bath
- customallowed to slowly reach 0° C
- filtrationThe precipitate was filtered
- washwashed with DCM
出典と根拠
- ORDレコード
- ord-d6b48ad051694d7791a681db44955dba
- 出典データセット
- uspto-grants-2010_05
- 特許番号
- US07713973B2
関連ノート
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