反応式
[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[N:5]=[C:4](Cl)[N:3]=1.[CH3:10][NH2:11]>>[NH2:1][C:2]1[N:7]=[C:6]([NH2:8])[N:5]=[C:4]([NH:11][CH3:10])[N:3]=1参加物
3
実験手順
A mixed solution comprising 14.5 g (0.1 mol) of 2,4-diamino-6-chloro-1,3,5-triazine synthesized in Reference Example 1 and 31.1 g (0.4 mol) of 40% aqueous solution of methylamine was heated under stirring and reacted finally at the reflux temperature thereof for 6 hours. After cooling the reacted solution, products were filtered off, and washed with cold water. The resulting filter residue was dried in vacuo at 70° C. for 6 hours to give 9.1 g (yield: 65%) of the titled compound. Malting point: 269° C.
後処理
- temperaturewas heated
- customreacted finally at the reflux temperature
- temperatureAfter cooling the reacted solution, products
- filtrationwere filtered off
- washwashed with cold water
- filtrationThe resulting filter residue
- customwas dried in vacuo at 70° C. for 6 hours
出典と根拠
- ORDレコード
- ord-db82ff322d4b4ffa9331772067bb510c
- 出典データセット
- uspto-grants-2005_04
- 特許番号
- US06878824B2
関連ノート
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