Diisopropylethylamine → HCID 23554393, 화합물

HRID 433450노트

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HRID 433450 반응식
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]

참가 물질

8

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-ed3d87efd580431ab011dd98531dae42
출처 데이터셋
uspto-grants-2003_12
특허 번호
US06667305B1

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