Thiophene → 4-(3-Aminophenyl)pyrimidin-2-amine
反応式
[N+:1]([C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][N:13]=[C:12]([NH2:16])[N:11]=2)[CH:7]=[CH:8][CH:9]=1)([O-])=O.S1C=CC=C1>CO.[Pd]>[NH2:1][C:4]1[CH:5]=[C:6]([C:10]2[CH:15]=[CH:14][N:13]=[C:12]([NH2:16])[N:11]=2)[CH:7]=[CH:8][CH:9]=1参加物
5
実験手順
4-(3-amino-phenyl)-pyrimidin-2-ylamine was prepared in an analogous manner: A solution of 4-(3-nitro-phenyl)-pyrimidin-2-ylamine (0.046 mol) in MeOH (250 ml) was hydrogenated at 50° C. with Pd/C 10% (2 g) as a catalyst in the presence of a solution of thiophene in DIPE (4% v/v, 1 ml). After uptake of H2 (3 equiv.), the catalyst was filtered off and the filtrate was concentrated and dried (vacuum 60° C.). Yield: 8.64g of 4-(3-amino-phenyl)-pyrimidin-2-ylamine (87%) (m.p.; 190-194° C.).
後処理
- filtrationAfter uptake of H2 (3 equiv.), the catalyst was filtered off
- concentrationthe filtrate was concentrated
- customdried (vacuum 60° C.)
出典と根拠
- ORDレコード
- ord-5c3def6ff28d4b578f26e39476d8db1a
- 出典データセット
- uspto-grants-2008_11
- 特許番号
- US07449465B2
反応ノート
読み込み中…