反応式
[Cl:1][C:2]1[CH:31]=[CH:30][CH:29]=[C:28]([Cl:32])[C:3]=1[C:4]([NH:6][C@H:7]([C:25](O)=[O:26])[CH2:8][C:9]1[CH:14]=[CH:13][C:12]([C:15]2[C:20]([O:21][CH3:22])=[CH:19][CH:18]=[CH:17][C:16]=2[O:23][CH3:24])=[CH:11][CH:10]=1)=[O:5].C1C=CC2N(O)N=NC=2C=1.CCN(C(C)C)C(C)C.[C:52]([CH2:54][CH2:55][NH2:56])#[N:53]>CN(C=O)C.O.C(Cl)CCl>[C:52]([CH2:54][CH2:55][NH:56][C:25](=[O:26])[C@H:7]([CH2:8][C:9]1[CH:10]=[CH:11][C:12]([C:15]2[C:20]([O:21][CH3:22])=[CH:19][CH:18]=[CH:17][C:16]=2[O:23][CH3:24])=[CH:13][CH:14]=1)[NH:6][C:4](=[O:5])[C:3]1[C:2]([Cl:1])=[CH:31][CH:30]=[CH:29][C:28]=1[Cl:32])#[N:53]参加物
8
反応物 4
生成物 1
試薬・触媒・溶媒 3
実験手順
A solution of N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxyphenyl)-L-phenylalanine (0.17 g), HOBT (0.0.08 g), DIEA (0.19 mL) and 2-cyanoethylamine (0.03 mL) in DMF (5 mL) was stirred at room temperature under N2. EDC (0.14 g) was added after 10 min and the mixture was stirred at room temperature under N2. The mixture was diluted with water and extracted with EtOAc. The extract was washed successively with water, 1 N HCl, satd. NaHCO3 and brine, dried and evaporated to give 0.17 g of N-(2,6-dichlorobenzoyl)-4-(2,6-dimethoxyphenyl)-L-phenylalanine N-(2-cyanoethyl)amide. ESMS: m/z 526 (MH+).
後処理
- extractionextracted with EtOAc
- washThe extract was washed successively with water, 1 N HCl
- dry with materialNaHCO3 and brine, dried
- customevaporated
出典と根拠
- ORDレコード
- ord-aff3e8797c4c4264b4026d0d5839a616
- 出典データセット
- uspto-grants-2005_02
- 特許番号
- US06855843B2
関連ノート
読み込み中…