Trifluoroacetic acid → 4-(2-fluoro-5-((1R)-1-((2S)-2-methyl-4-(methylsulfonyl)-1-piperazinyl)ethyl)-3-pyridinyl)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine

HRID 1621807노트

반응식

HRID 1621807 반응식
[CH3:1][O:2][C:3]1[CH:49]=[CH:48][C:6]([CH2:7][N:8]([CH2:39][C:40]2[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[CH:42][CH:41]=2)[C:9]2[N:14]=[C:13]([CH3:15])[N:12]=[C:11]([C:16]3[CH:17]=[C:18]([C@H:23]([N:25]4[CH2:30][CH2:29][N:28](C(OC(C)(C)C)=O)[CH2:27][C@@H:26]4[CH3:38])[CH3:24])[CH:19]=[N:20][C:21]=3[F:22])[N:10]=2)=[CH:5][CH:4]=1.C(O)(C(F)(F)F)=O.C([O-])(O)=O.[Na+].CCN(CC)CC.[CH3:69][S:70](Cl)(=[O:72])=[O:71]>C(Cl)Cl.O>[F:22][C:21]1[C:16]([C:11]2[N:12]=[C:13]([CH3:15])[N:14]=[C:9]([N:8]([CH2:39][C:40]3[CH:45]=[CH:44][C:43]([O:46][CH3:47])=[CH:42][CH:41]=3)[CH2:7][C:6]3[CH:48]=[CH:49][C:3]([O:2][CH3:1])=[CH:4][CH:5]=3)[N:10]=2)=[CH:17][C:18]([C@H:23]([N:25]2[CH2:30][CH2:29][N:28]([S:70]([CH3:69])(=[O:72])=[O:71])[CH2:27][C@@H:26]2[CH3:38])[CH3:24])=[CH:19][N:20]=1

참가 물질

8

반응물 5

HCID 6422Trifluoroacetic acidHCID 8471TriethylamineHCID 31297Methanesulfonyl chlorideHCID 516892Sodium Bicarbonate2회HCID 66611873tert-butyl (3S)-4-((1R)-1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-fluoro-3-pyridinyl)ethyl)-3-methyl-1-piperazinecarboxylate

생성물 1

HCID 666117444-(2-fluoro-5-((1R)-1-((2S)-2-methyl-4-(methylsulfonyl)-1-piperazinyl)ethyl)-3-pyridinyl)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine수율 84%

시약·촉매·용매 2

HCID 962Water용매HCID 6344Dichloromethane용매3회

실험 절차

A solution of tert-butyl (3S)-4-((1R)-1-(5-(4-(bis(4-methoxybenzyl)amino)-6-methyl-1,3,5-triazin-2-yl)-6-fluoro-3-pyridinyl)ethyl)-3-methyl-1-piperazinecarboxylate (9.17 g, 13.65 mmol) in CH2Cl2 (136 mL) at 0° C. was treated with TFA (52.6 mL, 682 mmol) (added over 10 min). The ice bath was then removed and the reaction mixture stirred at ambient temperature for 90 min. The solvent was removed in vacuo with a heating bath at 25° C., providing a viscous oil, which was cooled to 0° C. and diluted with 150 mL of CH2Cl2. Ice was added to the resulting solution, followed by solid NaHCO3 with rapid stirring until effervescence ceased. The resulting mixture was diluted with water (100 mL) and CH2Cl2 (150 mL). The organic layer was separated, and the aqueous layer was extracted with CH2Cl2 (2×). All organic layers were then combined, dried over sodium sulfate, and filtered through a 0.45 μm ZAPCAP filter (Whatman, Schleicher & Schuell). The filtrate was then concentrated to about 150 mL and cooled to 0° C. NEt3 (7.61 mL, 54.6 mmol) was added, followed by methanesulfonyl chloride (2.11 mL, 27.3 mmol). After 1 h at 0° C., saturated aqueous NaHCO3 was added and the resulting mixture was extracted with CH2Cl2 (3×). The combined organic extracts were dried over Na2SO4, filtered, and concentrated. The crude material was loaded onto a silica gel column (330 g) as a solution in CH2Cl2 and purified by column chromatography (20% to 100% (10% MeOH/EtOAc)/hexanes), which gave 4-(2-fluoro-5-((1R)-1-((2S)-2-methyl-4-(methylsulfonyl)-1-piperazinyl)ethyl)-3-pyridinyl)-N,N-bis(4-methoxybenzyl)-6-methyl-1,3,5-triazin-2-amine (7.45 g, 11.47 mmol, 84% yield) as an off-white foam. m/z (ESI, +ve) 650.2 (M+H)+. 1H NMR (400 MHz, CDCl3) δ 8.41-8.47 (m, 1H); 8.21-8.25 (m, 1H); 7.20-7.25 (m, 4H); 6.83-6.89 (m, 4H); 4.81 (d, J=8.61 Hz, 4H); 4.02 (q, J=6.78 Hz, 1H); 3.81 (s, 3H); 3.79 (s, 3H); 3.28-3.35 (m, 1H); 3.12-3.20 (m, 1H); 3.05-3.10 (m, 1H); 2.92-2.99 (m, 1H); 2.87 (ddd, J=11.44, 7.92, 3.33 Hz, 1H); 2.70 (s, 3H) 2.60-2.68 (m, 2H) 2.55 (s, 3H) 1.43 (d, J=6.85 Hz, 3H) 1.08 (d, J=6.46 Hz, 3H).

후처리

  1. customThe ice bath was then removed
  2. customThe solvent was removed in vacuo with a heating bath at 25° C.
  3. customproviding a viscous oil, which
  4. temperaturewas cooled to 0° C.
  5. additionIce was added to the resulting solution
  6. stirringwith rapid stirring until effervescence
  7. customThe organic layer was separated
  8. extractionthe aqueous layer was extracted with CH2Cl2 (2×)
  9. dry with materialdried over sodium sulfate
  10. filtrationfiltered through a 0.45 μm ZAPCAP
  11. filtrationfilter (Whatman, Schleicher & Schuell)
  12. concentrationThe filtrate was then concentrated to about 150 mL
  13. temperaturecooled to 0° C
  14. waitAfter 1 h at 0° C.
  15. extractionthe resulting mixture was extracted with CH2Cl2 (3×)
  16. dry with materialThe combined organic extracts were dried over Na2SO4
  17. filtrationfiltered
  18. concentrationconcentrated
  19. custompurified by column chromatography (20% to 100% (10% MeOH/EtOAc)/hexanes), which

출처 및 근거

ORD 기록
ord-640f879f3fdf472f93d26811dff9f799
출처 데이터셋
uspto-grants-2014_07
특허 번호
US08772480B2

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