Hydrochloric Acid → 5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline

HRID 74214

반응식

HRID 74214 반응식
F[C:2]1[CH:7]=[CH:6][C:5]([C:8]2[O:9][C:10]3[CH:16]=[CH:15][CH:14]=[C:13](C)[C:11]=3[N:12]=2)=[CH:4][C:3]=1[N+:18]([O-])=O.C([N:23]([CH2:26][CH3:27])CC)C.N[CH:29]1[CH2:34]CC[CH2:31][O:30]1.Cl.[H][H]>C(O)C.[C].[Pd].C(OCC)(=O)C.CO>[O:30]1[CH2:31][CH2:27][CH:26]([NH:23][C:2]2[CH:7]=[CH:6][C:5]([C:8]3[O:9][C:10]4[CH:16]=[CH:15][CH:14]=[CH:13][C:11]=4[N:12]=3)=[CH:4][C:3]=2[NH2:18])[CH2:34][CH2:29]1

참가 물질

9

반응물 5

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 14471248Oxan-2-amineHCID 674986872-Fluoro-5-(4-methylbenzoxazol-2-yl)nitrobenzeneHCID 178418361HCID 178418361, 화합물

생성물 1

HCID 674988065-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline수율 100.6%

시약·촉매·용매 3

HCID 178418390HCID 178418390, 화합물촉매HCID 702Ethanol용매HCID 21584119Ethylacetate methanol용매

실험 절차

To a suspension of 2-fluoro-5-(4-methylbenzoxazol-2-yl)nitrobenzene (see Working Example 46-1) (0.50 g, 1.8 mmol) in ethanol (10 mL) was added triethylamine (0.22 g, 2.17 mmol) and aminotetrahydropyran (0.20 g, 1.9 mmol), and this was heated to reflux for 3 hours. After the reaction was complete, this was cooled to room temperature and then the mixture was poured into dilute hydrochloric acid (1 M, 10 mL), this was extracted with chloroform (50 mL), and washed with saturated sodium hydrogen carbonate (approx. 50 mL) and then with brine (approx. 50 mL). The organic layer was dried over anhydrous magnesium sulfate, and then the solvent was distilled away at reduced pressure to give crystals, which were added to palladium-carbon (Pd: 10%, 0.06 g) and a solvent mixture of ethyl acetate/methanol (1:1, 20 mL), hydrogen was substituted in by successively reducing the pressure and purging with hydrogen gas 3 times, and this was stirred at room temperature for 2.5 hours. After substituting in nitrogen, the insoluble material was filtered off through a Celite layer (20 mm thickness), and this same layer was washed with methanol (20 mL, 3 times). The filtrate and wash solutions were combined and the solvent was distilled away under reduced pressure to yield the title compound (0.56 g, 94.3% yield) as a blackish brown solid.

후처리

  1. temperaturethis was heated
  2. temperatureto reflux for 3 hours
  3. extractionthis was extracted with chloroform (50 mL)
  4. washwashed with saturated sodium hydrogen carbonate (approx. 50 mL)
  5. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  6. distillationthe solvent was distilled away at reduced pressure
  7. customto give crystals, which
  8. custompurging with hydrogen gas 3 times
  9. filtrationthe insoluble material was filtered off through a Celite layer (20 mm thickness)
  10. washthis same layer was washed with methanol (20 mL, 3 times)
  11. washThe filtrate and wash solutions
  12. distillationthe solvent was distilled away under reduced pressure

출처 및 근거

ORD 기록
ord-213d9a60bed94ef6bba1a98743f8ea69
출처 데이터셋
uspto-grants-2014_09
특허 번호
US08829035B2

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