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Ammonium formate → 2-(Pyrrolidin-3-yl)pyridine

HRID 1757410
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HRID 1757410 반응식
C1(C[N:8]2[CH2:12][CH2:11][CH:10]([C:13]3[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=3)[CH2:9]2)C=CC=CC=1.C([O-])=O.[NH4+]>[Pd].CO.O>[NH:8]1[CH2:12][CH2:11][CH:10]([C:13]2[CH:18]=[CH:17][CH:16]=[CH:15][N:14]=2)[CH2:9]1
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참가 물질

6

반응물 2

HCID 2723923Ammonium formateHCID 109556222-(1-Benzylpyrrolidin-3-yl)pyridine

생성물 1

HCID 50139382-(Pyrrolidin-3-yl)pyridine수율 75%

시약·촉매·용매 3

HCID 23938Palladium촉매HCID 887Methanol용매HCID 962Water용매

실험 절차

To a suspension of 2-[1-(phenylmethyl)-3pyrrolidinyl]pyridine (7.15 g, 30.0mmol) and 10% palladium on charcoal catalyst (1.90 g) in methanol (120 mL) was added dropwise a solution of ammonium formate (7.57 g, 120 retool) in water (30 mL). The mixture was heated at reflux for 30 minutes, allowed tocool to room temperature, and filtered. The filtrate was concentrated underreduced pressure, the residue was taken up in water (10 mL), and the solution was made basic with concentrated ammonia and extracted with dichloromethane (4×15 mL). The organic extracts were combined, driedover anhydrous potassium carbonate, and concentrated to a yellow oil. This crude product was chromatographed (silica gel, chloroform-methanol-ammonia75:25:5) to give the title compound (3.33 g, 75%) as a faint yellow liquid.

후처리

  1. temperatureThe mixture was heated
  2. temperatureat reflux for 30 minutes
  3. customto room temperature
  4. filtrationfiltered
  5. concentrationThe filtrate was concentrated underreduced pressure
  6. extractionextracted with dichloromethane (4×15 mL)
  7. concentrationconcentrated to a yellow oil
  8. customThis crude product was chromatographed (silica gel, chloroform-methanol-ammonia75:25:5)

출처 및 근거

ORD 기록
ord-6aae8b198e094cf18556f7d211453ae1
출처 데이터셋
uspto-grants-1995_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05446044

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