反応式
[C:1]([O:5][C:6]([NH:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([OH:15])=O)=[C:11]([N+:18]([O-:20])=[O:19])[CH:10]=1)=[O:7])([CH3:4])([CH3:3])[CH3:2].C[N+:22](C)=C(N(C)C)ON1C2C=CC=CC=2N=N1.F[P-](F)(F)(F)(F)F.Cl.[C:46]([O:50][C:51](=[O:63])[C@H:52]([CH2:54][CH2:55][C:56]([O:58][C:59]([CH3:62])([CH3:61])[CH3:60])=[O:57])[NH2:53])([CH3:49])([CH3:48])[CH3:47]>ClCCl.C(N(CC)CC)C>[C:1]([O:5][C:6]([NH:8][C:9]1[CH:17]=[CH:16][C:12]([C:13]([NH:22][NH:53][C@H:52]([C:51]([O:50][C:46]([CH3:48])([CH3:49])[CH3:47])=[O:63])[CH2:54][CH2:55][C:56]([O:58][C:59]([CH3:62])([CH3:61])[CH3:60])=[O:57])=[O:15])=[C:11]([N+:18]([O-:20])=[O:19])[CH:10]=1)=[O:7])([CH3:2])([CH3:3])[CH3:4]参加物
反応物 3
生成物 1
試薬・触媒・溶媒 2
実験手順
To a mixture of 4-(tert-butoxycarbonylamino)-2-nitrobenzoic acid in 60 ml of dichloromethane were added 4.8 g of N,N,N′,N′-tetramethyl-O-(1H-benzotriazol-1-yl)-uronium-hexafluorophosphate. After stirring for 15 min. a mixture of 3.8 g of L-glutamic acid-di tert.-butylester hydrochloride in 60 ml dichloromethane and 3 ml triethylamine was added dropwise. After stirring for 20 hours at room temperature, the mixture was filtered and the filtrate was washed five times with 10% aqueous citric acid, four times with 5% aqueous sodium carbonate solution and two times with water. The organic layer was dried over magnesium sulphate and concentrated in vacuum to give 6.3 g of di-tert-butyl N-(4-(tert-butoxycarbonylamino)-2-nitrobenzamido)-L-glutamate as a yellow foam. This was directly used in example 3.
後処理
- additionwas added dropwise
- stirringAfter stirring for 20 hours at room temperature
- filtrationthe mixture was filtered
- washthe filtrate was washed five times with 10% aqueous citric acid, four times with 5% aqueous sodium carbonate solution and two times with water
- dry with materialThe organic layer was dried over magnesium sulphate
- concentrationconcentrated in vacuum
出典と根拠
- ORDレコード
- ord-5050c73064234dc0801cc0c6f60729b4
- 出典データセット
- uspto-grants-2016_04
- 特許番号
- US09315506B2
関連ノート
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