Hydrochloric Acid → HCID 60128225, 화합물

HRID 2307251노트

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HRID 2307251 반응식
Cl.[CH3:2][C@@H:3]1[CH2:8][CH2:7][NH:6][C@@H:5]([C:9]([OH:11])=[O:10])[CH2:4]1.[N:12]([O-])=O.[Na+].FC(F)(F)C(OC(=O)C(F)(F)F)=O>O.CCOCC>[CH3:2][C@@H:3]1[CH2:8][CH2:7][N+:6]2=[N:12][O:10][C:9]([O-:11])=[C:5]2[CH2:4]1

참가 물질

7

반응 조건

온도
-5 °C

실험 절차

Concentrated hydrochloric acid (6.0 ml) was added to a suspension of (2R,4R)-4-methyl-2-piperidinecarboxylic acid (Biochem. Biophys. Res. Commun. 1981; 101(2); 440) (10 g, 7.03 mmol), in water (30 ml) and this solution cooled to −5° C. A solution of sodium nitrite (5.3 g, 7.7 mmol), in water (20 ml) was then added, and this solution stirred at room temperature for 2 hours. The mixture was extracted with dichloromethane, twice, and the combined organic extracts were dried (MgSO4) and evaporated under reduced pressure to give a white solid. Trifluoroacetic anhydride (11 ml, 7.70 mmol) was added to a cooled (−3° C.) solution of the intermediate product in ether (200 ml) and the reaction stirred overnight at room temperature. The mixture was evaporated under reduced pressure, and the residue purified by column chromatography using ethyl acetate as the eluant. The title compound was obtained as a brown crystalline solid, 7.1 g.

후처리

  1. extractionThe mixture was extracted with dichloromethane
  2. dry with materialtwice, and the combined organic extracts were dried (MgSO4)
  3. customevaporated under reduced pressure
  4. customto give a white solid
  5. stirringthe reaction stirred overnight at room temperature
  6. customThe mixture was evaporated under reduced pressure
  7. customthe residue purified by column chromatography

출처 및 근거

ORD 기록
ord-3a4607a498ff4e0198a1ca37582c087d
출처 데이터셋
uspto-grants-2004_12
특허 번호
US06831074B2

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