反応式
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:22](=[O:23])[N:21]([CH3:24])[C:12]2[N:13]=[C:14](S(C)(=O)=O)[N:15]=[CH:16][C:11]=2[CH:10]=1.[NH2:25][C:26]1[CH:27]=[C:28]([CH:34]=[CH:35][CH:36]=1)[C:29]([O:31][CH2:32][CH3:33])=[O:30].C(O)(=O)C>O>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([Cl:8])[C:3]=1[C:9]1[C:22](=[O:23])[N:21]([CH3:24])[C:12]2[N:13]=[C:14]([NH:25][C:26]3[CH:27]=[C:28]([CH:34]=[CH:35][CH:36]=3)[C:29]([O:31][CH2:32][CH3:33])=[O:30])[N:15]=[CH:16][C:11]=2[CH:10]=1参加物
5
反応条件
- 温度
- 100 °C
実験手順
A mixture of 0.226 g (0.58 mmol) of 6-(2,6-dichlorophenyl)-2-methanesulfonyl-8-methyl-8H-pyrido[2,3-d]pyrimidin-7-one of Example 39 and 0.40 g (2.42 mmol) of 3-aminobenzoic acid, ethyl ester was fused in a 170° C. oil bath to give a clear melt. After 6 minutes, the melt was cooled to ca. 100° C. Glacial acetic acid (1 mL) was added to dissolve the melt. Water (5 mL) was added to precipitate a solid. The solid was filtered, washed well with water, and triturated with 2 mL of methanol. The mixture was filtered, and the cake was washed with 1 mL of methanol and then ether; wt 0.194 g. Recrystallization from ethyl acetate gave pure product; wt 0.075 g; mp 238°-240° C.
後処理
- customwas fused in a 170° C.
- customto give a clear melt
- dissolutionto dissolve the melt
- customto precipitate a solid
- filtrationThe solid was filtered
- washwashed well with water
- customtriturated with 2 mL of methanol
- filtrationThe mixture was filtered
- washthe cake was washed with 1 mL of methanol
- customRecrystallization from ethyl acetate
- customgave pure product
出典と根拠
- ORDレコード
- ord-9fd5cd2b22e5454fb149f6f3ed738293
- 出典データセット
- uspto-grants-1998_03
- 特許番号
- US05733914
関連ノート
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