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Hydrochloric Acid → HCID 44514686, 화합물

HRID 1931716
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HRID 1931716 반응식
[F:1][C:2]([F:8])([F:7])[C:3]([OH:6])([CH3:5])[CH3:4].Cl[C:10](Cl)([O:12]C(=O)OC(Cl)(Cl)Cl)Cl.Cl.FC(F)(F)C(O)=O.[CH3:29][S:30]([C:33]1[CH:54]=[CH:53][C:36]([O:37][C:38]2[N:43]=[CH:42][N:41]=[C:40]3[N:44]([CH:47]4[CH2:52][CH2:51][NH:50][CH2:49][CH2:48]4)[N:45]=[CH:46][C:39]=23)=[CH:35][CH:34]=1)(=[O:32])=[O:31].C(N(CC)CC)C.[Cl-].[NH4+]>N1C=CC=CC=1.C(OCC)C>[F:1][C:2]([F:8])([F:7])[C:3]([O:6][C:10]([N:50]1[CH2:49][CH2:48][CH:47]([N:44]2[C:40]3=[N:41][CH:42]=[N:43][C:38]([O:37][C:36]4[CH:35]=[CH:34][C:33]([S:30]([CH3:29])(=[O:32])=[O:31])=[CH:54][CH:53]=4)=[C:39]3[CH:46]=[N:45]2)[CH2:52][CH2:51]1)=[O:12])([CH3:5])[CH3:4]
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참가 물질

9

반응물 6

HCID 313Hydrochloric AcidHCID 8471TriethylamineHCID 25517Ammonium ChlorideHCID 681821,1,1-Trifluoro-2-methylpropan-2-olHCID 94429TriphosgeneHCID 669153264-(4-methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate salt2회

생성물 1

HCID 44514686
HCID 44514686, 화합물
수율 10%

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 3283Diethyl Ether용매

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온도
0 °C

실험 절차

A solution of 2-trifluoromethyl-2-propanol (Aldrich Chemical Company, Inc., Milwaukee, Wis., USA; 500 mg, 3.91 mmol) in pyridine (347 μL) was added to a cooled (0° C.) solution of triphosgene (386 mg, 1.3 mmol) in diethyl ether (35 mL). The mixture was stirred overnight and then 1 M aqueous hydrochloric acid (4 mL) was added. The organic layer was separated and washed with brine, dried (magnesium sulfate), filtered, and evaporated. The resulting material was dissolved in tetrahydrofuran (5 mL) and the solution was cooled to 0° C. 4-(4-Methanesulfonyl-phenoxy)-1-piperidin-4-yl-1H-pyrazolo[3,4-d]pyrimidine trifluoroacetate salt (Intermediate 27; 210 mg, 0.43 mmol) and triethylamine (560 μL, 4 mmol) were added. The mixture was stirred for 30 min and then poured into saturated aqueous ammonium chloride solution and extracted three times with ethyl acetate. The combined organic extracts were washed with brine, dried (magnesium sulfate), filtered, evaporated, and purified by column chromatography, eluting with 50% ethyl acetate/hexanes, to give 4-[4-(4-methanesulfonyl-phenoxy)-pyrazolo[3,4-d]pyrimidin-1-yl]-piperidine-1-carboxylic acid 2,2,2-trifluoro-1,1-dimethyl-ethyl ester (20.5 mg, 10%).

후처리

  1. customThe organic layer was separated
  2. washwashed with brine
  3. dry with materialdried (magnesium sulfate)
  4. filtrationfiltered
  5. customevaporated
  6. dissolutionThe resulting material was dissolved in tetrahydrofuran (5 mL)
  7. stirringThe mixture was stirred for 30 min
  8. extractionextracted three times with ethyl acetate
  9. washThe combined organic extracts were washed with brine
  10. dry with materialdried (magnesium sulfate)
  11. filtrationfiltered
  12. customevaporated
  13. custompurified by column chromatography
  14. washeluting with 50% ethyl acetate/hexanes

출처 및 근거

ORD 기록
ord-22066c956a4e4dd380f21aece0e86d1b
출처 데이터셋
uspto-grants-2012_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08188098B2

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