反応式
[CH3:1][C:2]1([CH3:24])[S:6]C(C(NC(CC2C=CC=CC=2)=O)C(O)=O)[NH:4][CH:3]1[C:21]([OH:23])=[O:22].COC1C=CC=C(N)C=1.C1(C)C=CC=CC=1.C(O)(=O)C>O>[NH2:4][C@@H:3]([C:21]([OH:23])=[O:22])[C:2]([SH:6])([CH3:24])[CH3:1]参加物
6
実験手順
3.52 g (0.01 mole) of benzylpenicilloic acid, 3.70 g (0.03 mole) of m-anisidine and 20 ml of toluene were added to a solution of 3.60 g (0.06mole) of acetic acid in 30 ml of water. The mixture was heated under reflux, with stirring, for 4 hours in a nitrogen atmosphere. The reaction mixture was then treated as described in Example 9 to give D-penicillamine as colorless crystals: yield 1.07 g (71.8%), m.p. 201°-202° C.
後処理
- temperatureThe mixture was heated
- temperatureunder reflux
- additionThe reaction mixture was then treated
出典と根拠
- ORDレコード
- ord-1311a4fdba864b7e9c27194c25e7fbda
- 出典データセット
- uspto-grants-1979_04
- 特許番号
- US04150240
関連ノート
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