Hydrogen Bromide → 2-(Pyridin-2-yl)benzene-1-sulfonamide
反応式
CC([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:20]=[CH:19][CH:18]=[CH:17][N:16]=1)(=[O:8])=[O:7])(C)C.Br>CO>[N:16]1[CH:17]=[CH:18][CH:19]=[CH:20][C:15]=1[C:10]1[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=1[S:6]([NH2:5])(=[O:7])=[O:8]参加物
4
実験手順
A solution of 14.8 g of the sulfonamide from Example 1 and 10 ml of 48% hydrobromic acid in 100 ml of methanol was heated at 40°-45° for 16 hours, concentrated, and neutralized wth aqueous sodium bicarbonate. The solid was filtered, washed with ice-water, and air-dried to afford 6.0 g of product, m.p. 186°-190°. NMR(CDCl3 /DMSO-d6)δ: 7.5 (m, 7), 8.1 (m, 2), 8.6 (d, 1). 1R(Nujol) 3300, 3260 cm-1. m/e M+ 234.
後処理
- concentrationconcentrated
- filtrationThe solid was filtered
- washwashed with ice-water
- customair-dried
出典と根拠
- ORDレコード
- ord-267c7130d42644039ce8f5f9fb1d3a5a
- 出典データセット
- uspto-grants-1985_01
- 特許番号
- US04494980
反応ノート
読み込み中…