Amino-1-(3-iodophenyl)-benzimidazole → 2-Amino-1-[3-(3-hydroxymethyl-4-thienyl)-phenyl]-benzimidazole
反応式
[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9](I)[CH:8]=2)[C:5]2[CH:14]=[CH:15][CH:16]=[CH:17][C:4]=2[N:3]=1.[OH:18][CH2:19][C:20]1[C:21](B(O)O)=[CH:22][S:23][CH:24]=1>>[NH2:1][C:2]1[N:6]([C:7]2[CH:12]=[CH:11][CH:10]=[C:9]([C:21]3[C:20]([CH2:19][OH:18])=[CH:24][S:23][CH:22]=3)[CH:8]=2)[C:5]2[CH:14]=[CH:15][CH:16]=[CH:17][C:4]=2[N:3]=1参加物
3
実験手順
2-Amino-1-[3-(3-hydroxymethyl-4-thienyl)-phenyl]-benzimidazole was synthesized as above with amino-1-(3-iodophenyl)-benzimidazole and 4-hydroxymethyl-3-thienylboronic acid as starting materials. Yield 56%, mp. 106°-108° C.
出典と根拠
- ORDレコード
- ord-d7d5482b94f94d5ba0f1d98b8ef7d33f
- 出典データセット
- uspto-grants-1995_08
- 特許番号
- US05441969
反応ノート
読み込み中…