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Methyl Isocyanate → HCID 18975131, 화합물

HRID 2393494
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HRID 2393494 반응식
[Br:1][C:2]1[CH:22]=[CH:21][C:5]2[CH2:6][CH:7]([CH3:20])[NH:8][N:9]=[C:10]([C:11]3[CH:16]=[CH:15][C:14]([N+:17]([O-:19])=[O:18])=[CH:13][CH:12]=3)[C:4]=2[CH:3]=1.[CH3:23][N:24]=[C:25]=[O:26]>C(O)C>[Br:1][C:2]1[CH:22]=[CH:21][C:5]2[CH2:6][CH:7]([CH3:20])[N:8]([C:25](=[O:26])[NH:24][CH3:23])[N:9]=[C:10]([C:11]3[CH:12]=[CH:13][C:14]([N+:17]([O-:19])=[O:18])=[CH:15][CH:16]=3)[C:4]=2[CH:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 12228Methyl IsocyanateHCID 18975181HCID 18975181, 화합물

생성물 1

HCID 18975131HCID 18975131, 화합물수율 84%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

0.84 g (2.33 mmoles) of 8-bromo-4-methyl-1-(4-nitrophenyl)-4,5-dihydro-3H-2,3-benzodiazepine (prepared in Example 22, Step D) are reacted with methyl isocyanate according to the method of Example 3. The crude product is suspended in 5 ml of hot ethanol. After filtration and drying, 0.82 g (84%) of the title compound are obtained. M.p.: 197°-200° C.

후처리

filtration
After filtration
  • customdrying
  • 출처 및 근거

    ORD 기록
    ord-d49cbbd90f594065bb0f1fdb8c23329a
    출처 데이터셋
    uspto-grants-1998_09
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US05807851

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