7-Chloro-2-iodothieno(3,2-b)pyridine → 5-(2,5-difluoro-4-(2-iodothieno[3,2-b]pyridin-7-yloxy)phenyl)-3-methyl-2-(phenylamino)pyrimidin-4(3H)-one

HRID 1676380노트

반응식

HRID 1676380 반응식
[F:1][C:2]1[CH:7]=[C:6]([OH:8])[C:5]([F:9])=[CH:4][C:3]=1[C:10]1[C:11](=[O:24])[N:12]([CH3:23])[C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:14][CH:15]=1.Cl[C:26]1[CH:31]=[CH:30][N:29]=[C:28]2[CH:32]=[C:33]([I:35])[S:34][C:27]=12>CN(C1C=CN=CC=1)C.BrC1C=CC=CC=1>[F:1][C:2]1[CH:7]=[C:6]([O:8][C:26]2[CH:31]=[CH:30][N:29]=[C:28]3[CH:32]=[C:33]([I:35])[S:34][C:27]=23)[C:5]([F:9])=[CH:4][C:3]=1[C:10]1[C:11](=[O:24])[N:12]([CH3:23])[C:13]([NH:16][C:17]2[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=2)=[N:14][CH:15]=1

참가 물질

5

실험 절차

A mixture of 5-(2,5-difluoro-4-hydroxyphenyl)-3-methyl-2-(phenylamino)pyrimidin-4(3H)-one (0.031 g, 0.093 mmol), 7-chloro-2-iodothieno[3,2-b]pyridine (0.025 g, 0.085 mmol; prepared according to the procedure of Ragan, J. A. Org. Proc. Res. 2003, 7, 676) and DMAP (0.010 g, 0.085 mmol) in bromobenzene (1.5 mL) under nitrogen was stirred at 150° C. for 6 days. The reaction was concentrated in vacuo to remove as much bromobenzene as possible and then purified directly by flash column chromatography, eluting with 20:1 CH2Cl2/MeOH. The product was obtained (10.5 mg; 21%) as a yellow solid. LRMS (APCI pos) m/e 589 (M+1).

후처리

  1. customprepared
  2. concentrationThe reaction was concentrated in vacuo
  3. customto remove as much bromobenzene as possible and
  4. customthen purified directly by flash column chromatography
  5. washeluting with 20:1 CH2Cl2/MeOH
  6. customThe product was obtained (10.5 mg; 21%) as a yellow solid

출처 및 근거

ORD 기록
ord-65a03d2f52804384ad161dcd2a80bd44
출처 데이터셋
uspto-grants-2011_08
특허 번호
US08003662B2

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