Hydrochloric Acid → 3-(N-[[trans 3-mercaptomethyl-2-oxo-1-azacylodecan-10-yl]-carbonyl]-amino)-pyridine hydrochloride
反応式
C([S:4][CH2:5][C@H:6]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][C@H:9]([C:16]([NH:18][C:19]2[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=2)=[O:17])[NH:8][C:7]1=[O:25])(=O)C.[ClH:26]>C(O)C>[ClH:26].[SH:4][CH2:5][C@H:6]1[CH2:15][CH2:14][CH2:13][CH2:12][CH2:11][CH2:10][C@H:9]([C:16]([NH:18][C:19]2[CH:20]=[N:21][CH:22]=[CH:23][CH:24]=2)=[O:17])[NH:8][C:7]1=[O:25]参加物
実験手順
3-{N-[[trans 3-(acetylthiomethyl)-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino}-pyridine (0.040 g, 0.11 mmol) is dissolved in ethanol (1.0 mL). An aqueous solution of nitrogen-degasded 1N sodium hydroxide (0.33 mL, 0.33 mmol) is added, and the reaction is stirred for 90 minutes. The reaction is quenched with 1N hydrochloric acid (0.33 mL, 0.33 mmol), and the solvent is evaporated. The residue is partitioned between ethyl acetate and water, and the aqueous layer is extracted several times with ethyl acetate. The combined organic layers are dried (MgSO4), and the solvent is evaporated. The residue is dissolved in methylene chloride (5.0 mL), and anhydrous hydrochloric acid gas is bubbled through the reaction for 5 minutes. The solvent is evaporated to give 3-{N-[[trans 3-mercaptomethyl-2-oxo-1-azacyclodecan-10-yl]-carbonyl]-amino}-pyridine hydrochloride, MS: M+1=322.
後処理
- customthe solvent is evaporated
- customThe residue is partitioned between ethyl acetate and water
- extractionthe aqueous layer is extracted several times with ethyl acetate
- dry with materialThe combined organic layers are dried (MgSO4)
- customthe solvent is evaporated
- dissolutionThe residue is dissolved in methylene chloride (5.0 mL)
- customanhydrous hydrochloric acid gas is bubbled through the reaction for 5 minutes
- customThe solvent is evaporated
出典と根拠
- ORDレコード
- ord-039d993767fd48bca5979ee161469481
- 出典データセット
- uspto-grants-1993_09
- 特許番号
- US05244889
反応ノート
読み込み中…