Triethylamine → HCID 21890853, 화합물

HRID 721463노트

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HRID 721463 반응식
[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:22]=[CH:21][C:19]([NH2:20])=[C:18]([CH3:23])[C:17]=1[CH3:24].C([N:27](CC)CC)C.[C:32](Cl)(Cl)=[S:33].[CH2:36]([N:40]([CH2:45][CH2:46][CH2:47][CH3:48])[CH2:41][CH:42](N)[CH3:43])[CH2:37][CH2:38][CH3:39]>CN(C)C=O.C(OCC)(=O)C>[CH3:1][O:2][C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][C:12]=1[O:13][CH3:14])[N:9]=[CH:8][CH:7]=[C:6]2[O:15][C:16]1[CH:22]=[CH:21][C:19]([NH:20][C:32]([NH:27][CH2:43][CH2:42][CH2:41][N:40]([CH2:36][CH2:37][CH2:38][CH3:39])[CH2:45][CH2:46][CH2:47][CH3:48])=[S:33])=[C:18]([CH3:23])[C:17]=1[CH3:24]

참가 물질

7

실험 절차

4-[(6,7-Dimethoxy-4-quinolyl)oxy]-2,3-dimethylaniline (51 mg) was dissolved in N,N-dimethylformamide (2 ml) and triethylamine (1 ml) to prepare a solution. Thiophosgene (51 mg) was then added to the solution, and the mixture was stirred at room temperature for 6 hr. Next, N,N-dibutylpropylenediamine (50 mg) was added thereto, and the mixture was further stirred at room temperature for 15 hr. Ethyl acetate was added to the reaction solution, followed by washing with water and saturated brine in that order. The organic layer was then dried over anhydrous sodium sulfate. The solvent was removed by distillation under the reduced pressure, and the residue was purified by HPLC using chloroform/methanol for development to give the title compound (33 mg, yield 37%).

후처리

  1. stirringthe mixture was further stirred at room temperature for 15 hr
  2. washby washing with water and saturated brine in that order
  3. dry with materialThe organic layer was then dried over anhydrous sodium sulfate
  4. customThe solvent was removed by distillation under the reduced pressure
  5. customthe residue was purified by HPLC

출처 및 근거

ORD 기록
ord-d569792d33d848ee94793bf64836cc47
출처 데이터셋
uspto-grants-2006_11
특허 번호
US07135466B2

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