Furo[3,2-c]pyridine → Furo[2,3-c]pyridine-2-sulfonamide
反応式
[S:1]([C:5]1[O:13][C:12]2[CH:11]=CN=[CH:8][C:7]=2[CH:6]=1)(=[O:4])(=[O:3])[NH2:2].O1C2=[CH:19][N:20]=CC=C2C=C1.O1C2C=CN=CC=2C=C1>>[S:1]([C:5]1[O:13][C:12]2=[CH:11][N:20]=[CH:19][CH:8]=[C:7]2[CH:6]=1)(=[O:3])(=[O:4])[NH2:2]参加物
4
実験手順
The title compound was prepared according to the procedure described for the preparation of 2-sulfamoylfuro[3,2-c]pyridine except furo[2,3-c]pyridine was substituted for furo[3,2-c]pyridine. This compound was obtained in 40% yield after recrystallization from ethyl acetate, m.p. 199°-201° C.
後処理
- customThis compound was obtained in 40% yield
- customafter recrystallization from ethyl acetate, m.p. 199°-201° C.
出典と根拠
- ORDレコード
- ord-d539447e1cdc416ebfae463b03319aaa
- 出典データセット
- uspto-grants-1989_02
- 特許番号
- US04808595
反応ノート
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