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Ethyl isocyanate → HCID 67109704, 화합물

HRID 2370991
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HRID 2370991 반응식
[CH3:1][O:2][C:3]1[CH:8]=[CH:7][C:6]([C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[CH:15][CH:16]=3)[NH:11][C:10]=2[C:18]2[C:19]([CH3:24])=[N:20][O:21][C:22]=2[CH3:23])=[CH:5][CH:4]=1.[N:25]([CH2:28][CH3:29])=[C:26]=[O:27]>CN(C=O)C>[CH3:24][C:19]1[C:18]([C:10]2[N:11]([C:26]([NH:25][CH2:28][CH3:29])=[O:27])[C:12]3[C:17]([C:9]=2[C:6]2[CH:5]=[CH:4][C:3]([O:2][CH3:1])=[CH:8][CH:7]=2)=[CH:16][CH:15]=[CH:14][CH:13]=3)=[C:22]([CH3:23])[O:21][N:20]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 8022Ethyl isocyanate2회HCID 67108903HCID 67108903, 화합물

생성물 1

HCID 67109704HCID 67109704, 화합물

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
70 °C

실험 절차

4-(3-(4-methoxyphenyl)-1H-indol-2-yl)-3,5-dimethylisoxazole (15 mg, 0.06 mmol) and isocyanatoethane (40 μl) were mixed 1 ml dry DMF under nitrogen. The mixture was heated at 70° C. for 3 h. 100 μl isocyanatoethane were added and the heating at 70° C. continued over night. The crude reaction mixture was purified by prep HPLC. 8.0 mg 2-(3,5-dimethylisoxazol-4-yl)-N-ethyl-3-(4-methoxyphenyl)-1H-indole-1-carboxamide was obtained.

후처리

  1. waitthe heating at 70° C. continued over night
  2. customThe crude reaction mixture
  3. customwas purified by prep HPLC

출처 및 근거

ORD 기록
ord-35929eebde0c4247817cc77c81a3a1e0
출처 데이터셋
uspto-grants-2014_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08710243B2

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