HCID 66959554, 화합물 → HCID 59170751, 화합물

HRID 2247547노트

반응식

HRID 2247547 반응식
[C:1]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:8][C:9](=[O:36])/[C:10](=[CH:21]/[C:22]2[CH:27]=[CH:26][C:25]([N:28]3[CH:32]=[C:31]([CH3:33])[N:30]=[CH:29]3)=[C:24]([O:34][CH3:35])[CH:23]=2)/[CH2:11][CH2:12][CH2:13][O:14]C2CCCCO2)[CH:2]=1>CO>[C:1]1([C:37]2[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=2)[CH:6]=[CH:5][CH:4]=[C:3]([CH2:7][NH:8][C:9](=[O:36])/[C:10](=[CH:21]/[C:22]2[CH:27]=[CH:26][C:25]([N:28]3[CH:32]=[C:31]([CH3:33])[N:30]=[CH:29]3)=[C:24]([O:34][CH3:35])[CH:23]=2)/[CH2:11][CH2:12][CH2:13][OH:14])[CH:2]=1

참가 물질

3

반응물 1

HCID 66959554HCID 66959554, 화합물

생성물 1

HCID 59170751HCID 59170751, 화합물수율 83.9%

시약·촉매·용매 1

HCID 887Methanol용매

반응 조건

온도
45 °C

실험 절차

To the methanol (5 mL) solution of (E)-2-(3-methoxy-4-(4-methyl-1H-imidazol-1-yl)benzylidene)-5-(tetrahydropyran-2-yloxy)valeric acid (biphenyl-3-ylmethyl)amide (168 mg), Dow-XM50W X-8 (300 mg) was added, and the reaction solution was agitated at 45° C. for 5 hours. The resin was filtered off, the ammonia water (1 mL) was added to the filtrate, and the solution was concentrated under reduced pressure. The residue was purified by silica gel chromatography (elution solvent: ethyl acetate->ethyl acetate:methanol=9:1), and 120 mg of the title compound was obtained. The physical properties of the compound are as follows.

후처리

  1. addition(300 mg) was added
  2. filtrationThe resin was filtered off
  3. additionthe ammonia water (1 mL) was added to the filtrate
  4. concentrationthe solution was concentrated under reduced pressure
  5. customThe residue was purified by silica gel chromatography (elution solvent: ethyl acetate->ethyl acetate:methanol=9:1)

출처 및 근거

ORD 기록
ord-957137ee1c8740a5adf5d323dd0953a1
출처 데이터셋
uspto-grants-2010_03
특허 번호
US07687640B2

반응 노트

불러오는 중…