Diisopropylethylamine → HCID 23554393、化合物

HRID 411405ノート

反応式

HRID 411405 の反応式
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

8

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

  1. stirringstirred overnight
  2. extractionextracted sequentially with 10% citric acid, saturated sodium bicarbonate, water and brine
  3. dry with materialdried over sodium sulfate
  4. 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

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