Dimethyl acetylenedicarboxylate → Dimethyl-2-{[(amino-{(2S)-1-[(benzyloxy)carbonyl]-4,4-difluoropyrrolidin-2-yl}methylidene)amino]oxy}but-2-enedioate
反応式
[CH2:1]([O:8][C:9]([N:11]1[CH2:15][C:14]([F:17])([F:16])[CH2:13][C@H:12]1[C:18]([NH2:21])=[N:19][OH:20])=[O:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[CH3:22][O:23][C:24]([C:26]#[C:27][C:28]([O:30][CH3:31])=[O:29])=[O:25]>C(Cl)(Cl)Cl>[CH3:22][O:23][C:24](=[O:25])[C:26]([O:20][N:19]=[C:18]([NH2:21])[C@@H:12]1[CH2:13][C:14]([F:17])([F:16])[CH2:15][N:11]1[C:9]([O:8][CH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[CH:6][CH:7]=1)=[O:10])=[CH:27][C:28]([O:30][CH3:31])=[O:29]参加物
4
反応物 2
生成物 1
試薬・触媒・溶媒 1
実験手順
A solution of benzyl-(2S)-2-[amino(hydroxyimino)methyl]-4,4-difluoropyrrolidine-1-carboxylate and dimethylacetylendicarboxylate (1.2 eq.) in chloroform was refluxed for 1 hour under nitrogen and the solution was concentrated. Residue was purified by flash chromatography on silica gel, (eluent: petroleum ether:ethyl acetate=7.5:2.5), to give the desired product as a 3:1 mixture of two isomers by 1H NMR.
後処理
- concentrationthe solution was concentrated
- customResidue was purified by flash chromatography on silica gel, (eluent: petroleum ether:ethyl acetate=7.5:2.5),
出典と根拠
- ORDレコード
- ord-8be7dc4d537a408d955ca608a4268c17
- 出典データセット
- uspto-grants-2008_10
- 特許番号
- US07435734B2
反応ノート
読み込み中…