Sodium Iodide → Cyclohexanecarboxylic acid 5-{(4-{amino[2,2-dimethylpropoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester

HRID 2089640노트

반응식

HRID 2089640 반응식
[CH3:1][C:2]([CH3:46])([CH3:45])[CH2:3][O:4][C:5](=[O:44])[N:6]=[C:7]([NH2:43])[C:8]1[CH:13]=[CH:12][C:11]([NH:14][CH:15]([C:29]2[N:33]=[C:32]([O:34][CH2:35]Cl)[N:31]([C:37]3[N:42]=[CH:41][CH:40]=[CH:39][N:38]=3)[N:30]=2)[C:16]2[CH:21]=[C:20]([O:22][CH3:23])[CH:19]=[C:18]([O:24][CH2:25][CH2:26][OH:27])[C:17]=2[F:28])=[CH:10][CH:9]=1.C(=O)([O-])O.[K+].[I-].[Na+].[CH:54]1([C:60]([OH:62])=[O:61])[CH2:59][CH2:58][CH2:57][CH2:56][CH2:55]1.[Cl-].[NH4+]>CN(C=O)C>[NH2:43][C:7](=[N:6][C:5]([O:4][CH2:3][C:2]([CH3:46])([CH3:45])[CH3:1])=[O:44])[C:8]1[CH:13]=[CH:12][C:11]([NH:14][CH:15]([C:16]2[CH:21]=[C:20]([O:22][CH3:23])[CH:19]=[C:18]([O:24][CH2:25][CH2:26][OH:27])[C:17]=2[F:28])[C:29]2[N:33]=[C:32]([O:34][CH2:35][O:62][C:60]([CH:54]3[CH2:59][CH2:58][CH2:57][CH2:56][CH2:55]3)=[O:61])[N:31]([C:37]3[N:42]=[CH:41][CH:40]=[CH:39][N:38]=3)[N:30]=2)=[CH:10][CH:9]=1

참가 물질

7

반응물 5

HCID 5238Sodium IodideHCID 7413Cyclohexanecarboxylic acidHCID 25517Ammonium ChlorideHCID 516893Potassium BicarbonateHCID 67470504[1-amino-1-[4-({(5-chloromethoxy-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}amino)phenyl]methylidene]carbamic acid 2,2-dimethylpropyl ester

생성물 1

HCID 68212832Cyclohexanecarboxylic acid 5-{(4-{amino[2,2-dimethylpropoxycarbonylimino]methyl}phenylamino)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}-2-pyrimidin-2-yl-2H-[1,2,4]triazol-3-yloxymethyl ester수율 89.9%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

반응 조건

온도
45 °C

실험 절차

To a mixture of [1-amino-1-[4-({(5-chloromethoxy-1-pyrimidin-2-yl-1H-[1,2,4]triazol-3-yl)-[2-fluoro-3-(2-hydroxyethoxy)-5-methoxyphenyl]methyl}amino)phenyl]methylidene]carbamic acid 2,2-dimethylpropyl ester (Example 2b, 120 mg), potassium hydrogen carbonate (131 mg), and DMF (16 mL), sodium iodide (140 mg) and cyclohexanecarboxylic acid (163 mg) were added, and the resulting mixture was stirred at 45° C. overnight. After cooling the reaction mixture to room temperature, ice and saturated aqueous ammonium chloride solution were added thereto, and the resulting mixture was extracted three times with a mixture of THF and ethyl acetate. The organic layer was collected, washed with saturated aqueous ammonium chloride solution, and dried over anhydrous magnesium sulfate. The resulting mixture was filtered, and the filtrate obtained was concentrated under reduced pressure. The residue obtained was purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate) to obtain the captioned compound (123 mg).

후처리

  1. additionwere added
  2. temperatureAfter cooling the reaction mixture to room temperature
  3. extractionthe resulting mixture was extracted three times
  4. additionwith a mixture of THF and ethyl acetate
  5. customThe organic layer was collected
  6. washwashed with saturated aqueous ammonium chloride solution
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationThe resulting mixture was filtered
  9. customthe filtrate obtained
  10. concentrationwas concentrated under reduced pressure
  11. customThe residue obtained
  12. customwas purified by NAM silica gel column chromatography (mixed solvent of methanol-ethyl acetate)

출처 및 근거

ORD 기록
ord-2cb65d0adad14198a63a76085802c814
출처 데이터셋
uspto-grants-2013_05
특허 번호
US08436009B2

반응 노트

불러오는 중…