反応式
[C:1]1(=[O:21])[N:5]([CH2:6][CH2:7][CH2:8][O:9][C:10]2[CH:15]=[CH:14][N:13]=[CH:12][CH:11]=2)[C:4](=[O:16])[C:3]2=[CH:17][CH:18]=[CH:19][CH:20]=[C:2]12.[ClH:22].CO>CO>[ClH:22].[C:4]1(=[O:16])[N:5]([CH2:6][CH2:7][CH2:8][O:9][C:10]2[CH:11]=[CH:12][N:13]=[CH:14][CH:15]=2)[C:1](=[O:21])[C:2]2=[CH:20][CH:19]=[CH:18][CH:17]=[C:3]12参加物
4
実験手順
To a solution of 1.41 g (5.0 mmol) of 4-(3-phthalimidopropyloxy)pyridine in 20 ml of methanol, 10 ml of hydrogen chloride-methanol was added. The solvent was distilled off and acetone was added to the residue. The resulting crystals were collected by filtration and washed with acetone to give 1.03 g of the desired compound (64.8% yield, colorless crystals), mp. 167°-169° C.
後処理
- distillationThe solvent was distilled off
- additionacetone was added to the residue
- filtrationThe resulting crystals were collected by filtration
- washwashed with acetone
出典と根拠
- ORDレコード
- ord-c962e1c87c844b4594420eb59c04a717
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05246948
関連ノート
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