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Pyridine → 3-{4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-phenyl}-4H-[1,2,4]oxadiazol-5-one

HRID 1441690
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반응식

HRID 1441690 반응식
[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[N:10]([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:11][CH2:12][C:13]1[CH:22]=[CH:21][C:16]([C:17]([NH:19][OH:20])=[NH:18])=[CH:15][CH:14]=1.N1C=CC=CC=1.[C:33]1([O:39]C(Cl)=O)C=CC=CC=1.N12CCCN=C1CCCCC2>ClCCl.C(#N)C>[O:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[N:10]([CH2:23][CH2:24][CH2:25][CH3:26])[CH2:11][CH2:12][C:13]1[CH:22]=[CH:21][C:16]([C:17]2[NH:18][C:33](=[O:39])[O:20][N:19]=2)=[CH:15][CH:14]=1
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참가 물질

7

반응물 4

HCID 1049PyridineHCID 15891Phenyl chloroformateHCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 178449016HCID 178449016, 화합물

생성물 1

HCID 1361288833-{4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-phenyl}-4H-[1,2,4]oxadiazol-5-one

시약·촉매·용매 2

HCID 6342
Acetonitrile
용매
HCID 6344Dichloromethane용매

실험 절차

280 mg 4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-N-hydroxy-benzamidine were dissolved in 5 ml dichloromethane. 78 μl pyridine and 120 μl phenylchloroformate were added and the mixture stirred at room temperature for ten minutes. The mixture was diluted by the addition of 15 ml acetonitrile and 115 μl ml 1,8-Diazabicyclo[5.4.0]undec-7-ene were added. The mixture was stirred at room temperature for 10 minutes. The mixture was evaporated in vacuo and the resulting crude material was purified by reversed phase HPLC to obtain 105 mg 3-{4-[2-(Benzooxazol-2-yl-butyl-amino)-ethyl]-phenyl}-4H-[1,2,4]oxadiazol-5-one as an amorphous lyophilisate.

후처리

  1. additionwere added
  2. stirringThe mixture was stirred at room temperature for 10 minutes
  3. customThe mixture was evaporated in vacuo
  4. customthe resulting crude material was purified by reversed phase HPLC

출처 및 근거

ORD 기록
ord-f99f8cb3233c4709940f4230b9a849d3
출처 데이터셋
uspto-grants-2010_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07655679B2

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