Diisopropylethylamine → HCID 23554393、化合物
反応式
C1C=CC2N(O)N=NC=2C=1.O.C(N(CC)C(C)C)(C)C.[CH3:21][C@H:22]([NH:26][C:27]([O:29][C:30]([CH3:33])([CH3:32])[CH3:31])=[O:28])[C:23]([OH:25])=O.Cl.CN(C)CCCN=C=NCC.[NH2:46][CH:47]1[N:53]=[C:52]([C:54]2[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=2)[C:51]2[CH:60]=[CH:61][CH:62]=[CH:63][C:50]=2[N:49]([CH2:64][CH2:65][CH2:66][C:67]([F:70])([F:69])[F:68])[C:48]1=[O:71]>C1COCC1.C(Cl)Cl>[C:30]([O:29][C:27]([NH:26][C@H:22]([C:23]([NH:46][CH:47]1[N:53]=[C:52]([C:54]2[CH:55]=[CH:56][CH:57]=[CH:58][CH:59]=2)[C:51]2[CH:60]=[CH:61][CH:62]=[CH:63][C:50]=2[N:49]([CH2:64][CH2:65][CH2:66][C:67]([F:69])([F:68])[F:70])[C:48]1=[O:71])=[O:25])[CH3:21])=[O:28])([CH3:33])([CH3:32])[CH3:31]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a solution of HOBt-H2O (373 mg, 2.76 mmol), N,N-diisopropylethylamine (481 uL, 2.76 mmol) and N-t-BOC-L-alanine (522 mg, 2.76 mmol) in 10 mL of anhydrous THF at 0° C. was added 1-(3-dimethylaminopropyl)-3-ethyl carbodiimide hydrochloride (EDCI; 527 mg, 2.76 mmol) in one portion. After stirring 5 min., a solution of 3-amino-2,3-dihydro-1-(4,4,4-trifluorobutyl)-5-phenyl-1H-1,4-benzodiazepin-2-one (1.05 g, 2.91 mmol) in 10 mL of anhydrous THF was added via syringe and the reaction mixture was warmed to room temperature and stirred overnight. The reaction mixture was diluted with 100 mL methylene chloride, extracted sequentially with 10% citric acid, saturated sodium bicarbonate, water and brine and then dried over sodium sulfate. Purification of the crude product using silica gel chromatography (10%-30% ethyl acetate/methylene chloride) gave 1.28 g (83%) of a white foam.
後処理
- stirringstirred overnight
- extractionextracted sequentially with 10% citric acid, saturated sodium bicarbonate, water and brine
- dry with materialdried over sodium sulfate
- customPurification of the crude product
出典と根拠
- ORDレコード
- ord-4ca68b1ff87d4d5cb1d80977ead5e04c
- 出典データセット
- uspto-grants-2003_05
- 特許番号
- US06559141B2
反応ノート
読み込み中…