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N-bromobutanimide → HCID 10177162, 화합물

HRID 1057372
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HRID 1057372 반응식
[C:1]([O:5][C:6]([CH:8]1[CH2:14][CH2:13][C:12]2[CH:15]=[CH:16][C:17]([O:19][CH3:20])=[CH:18][C:11]=2[NH:10][C:9]1=[O:21])=[O:7])([CH3:4])([CH3:3])[CH3:2].C1C(=O)N([Br:29])C(=O)C1>C(O)(=O)C.C(Cl)(Cl)Cl.C(Cl)Cl>[Br:29][C:16]1[C:17]([O:19][CH3:20])=[CH:18][C:11]2[NH:10][C:9](=[O:21])[CH:8]([C:6]([O:5][C:1]([CH3:4])([CH3:3])[CH3:2])=[O:7])[CH2:14][CH2:13][C:12]=2[CH:15]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 2

HCID 67184N-bromobutanimideHCID 9857210HCID 9857210, 화합물

생성물 1

HCID 10177162HCID 10177162, 화합물

시약·촉매·용매 3

HCID 176Acetic Acid용매HCID 6212Chloroform용매HCID 6344Dichloromethane용매

실험 절차

A suspension of 3-tert-butoxycarbonyl-8-methoxy-2,3,4,5-tetrahydro-1H-1-benzazepine-2-one (1.00 g, 3.43 mmol) and NBS (0.672 g, 3.78 mmol) in acetic acid (0.8 mL) and chloroform (8 mL) was heated at reflux for 3 hrs. Then, the reaction mixture was diluted with DCM (30 mL), washed with water, dried over Na2SO4, filtered and evaporated. The crude residue was purified by flash chromatography on silica column using gradient elution with EtOAc/DCM (from 5% ethyl acetate in DCM to 10% ethyl acetate in DCM). The title compound was obtained as a white powder (0.689 g, 54%).

후처리

  1. temperaturewas heated
  2. temperatureat reflux for 3 hrs
  3. washwashed with water
  4. dry with materialdried over Na2SO4
  5. filtrationfiltered
  6. customevaporated
  7. customThe crude residue was purified by flash chromatography on silica column
  8. washelution with EtOAc/DCM (from 5% ethyl acetate in DCM to 10% ethyl acetate in DCM)

출처 및 근거

ORD 기록
ord-42866014304c4d729ddac88cb881817c
출처 데이터셋
uspto-grants-2003_02
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06514965B1

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