Hydrochloric Acid → HCID 60128225、化合物

HRID 2307251ノート

反応式

HRID 2307251 の反応式
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

参加物

7

反応条件

温度
-5 °C

実験手順

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.

後処理

  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

出典と根拠

ORDレコード
ord-3a4607a498ff4e0198a1ca37582c087d
出典データセット
uspto-grants-2004_12
特許番号
US06831074B2

反応ノート

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