Methyl bromoacetate → [4-(3-Benzo[d]isoxazolylimino)-1-(4H)-pyridinyl]-acetic acid methyl ester hydrobromide

HRID 2149

반응식

HRID 2149 반응식
[N:1]1[CH:6]=[CH:5][C:4]([NH:7][C:8]2[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[O:10][N:9]=2)=[CH:3][CH:2]=1.[Br:17][CH2:18][C:19]([O:21][CH3:22])=[O:20]>C(#N)C>[BrH:17].[CH3:22][O:21][C:19](=[O:20])[CH2:18][N:1]1[CH:2]=[CH:3][C:4](=[N:7][C:8]2[C:12]3[CH:13]=[CH:14][CH:15]=[CH:16][C:11]=3[O:10][N:9]=2)[CH:5]=[CH:6]1

참가 물질

4

반응물 2

HCID 60984Methyl bromoacetateHCID 98372191,2-Benzisoxazol-3-amine, N-4-pyridinyl-

생성물 1

HCID 70280625[4-(3-Benzo[d]isoxazolylimino)-1-(4H)-pyridinyl]-acetic acid methyl ester hydrobromide수율 70%

시약·촉매·용매 1

HCID 6342Acetonitrile용매

실험 절차

A mixture of 3-(4-pyridinylamino)-1,2-benzisoxazole (0.9 g, 4.3 mmol) and methyl bromoacetate (0.44 mL, 1.1 eq) in acetonitrile (25 mL) was heated at reflux for one hour. The mixture was then allowed to cool to room temperature and the precipitated product was collected by filtration. The white solid was washed with diethyl ether and dried under vacuum to provide the title compound (1.1 g, 70%), mp 235-236° C.

후처리

  1. temperaturewas heated
  2. temperatureat reflux for one hour
  3. filtrationthe precipitated product was collected by filtration
  4. washThe white solid was washed with diethyl ether
  5. customdried under vacuum

출처 및 근거

ORD 기록
ord-dc610c599a6a47cbbab5dcc6ac8c553a
출처 데이터셋
uspto-grants-1998_03
특허 번호
US05728717

연결된 노트

불러오는 중…