Thiourea → HCID 59790146, 화합물

HRID 1963733노트

반응식

HRID 1963733 반응식
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][C:3]=1[N:12]=[C:13]=S.[NH2:15][C:16]1[CH:17]=[C:18]([CH:37]=[CH:38][C:39]=1[NH:40][CH3:41])[O:19][C:20]1[CH:25]=[CH:24][N:23]=[C:22]([NH:26][C:27](=[O:36])[CH2:28][N:29]2[CH2:33][CH2:32][CH2:31][CH:30]2[CH2:34][OH:35])[CH:21]=1.NC(N)=S>CO>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([F:11])([F:10])[F:9])=[CH:4][C:3]=1[NH:12][C:13]1[N:40]([CH3:41])[C:39]2[CH:38]=[CH:37][C:18]([O:19][C:20]3[CH:25]=[CH:24][N:23]=[C:22]([NH:26][C:27](=[O:36])[CH2:28][N:29]4[CH2:33][CH2:32][CH2:31][C@H:30]4[CH2:34][OH:35])[CH:21]=3)=[CH:17][C:16]=2[N:15]=1

참가 물질

5

실험 절차

2-Fluoro-5-(trifluoromethyl)phenyl isothiocyanate was added to a solution of N-[4-(3-Amino-4-methylamino-phenoxy)-pyridin-2-yl]-2-(2-hydroxymethyl-pyrrolidin-1-yl)-acetamide in methanol. Reaction was stirred at room temperature for 15 hours. Thiourea formation was confirmed by LC/MS. Ferric chloride was added and the resulting mixture was stirred at room temperature for 4 hours. After cyclization was complete by LC/MS the reaction mixture was concentrated and aqueous sodium carbonate was added until basic pH. The reaction mixture was partitioned between ethyl acetate and water. The organic layer was washed with water then brine, and dried over magnesium sulfate and concentrated. The crude product was purified by reverse phase HPLC. MS: MH+=559.3.

후처리

  1. customReaction
  2. stirringthe resulting mixture was stirred at room temperature for 4 hours
  3. concentrationwas concentrated
  4. additionaqueous sodium carbonate was added until basic pH
  5. customThe reaction mixture was partitioned between ethyl acetate and water
  6. washThe organic layer was washed with water
  7. dry with materialbrine, and dried over magnesium sulfate
  8. concentrationconcentrated
  9. customThe crude product was purified by reverse phase HPLC

출처 및 근거

ORD 기록
ord-4897f81dc2f84791b2b061568b328181
출처 데이터셋
uspto-grants-2013_04
특허 번호
US08415382B2

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