Potassium Carbonate → (2S,3'S)-2-Methyl-1'-(6-nitro-pyridin-3-yl)-[1,3']bipyrrolidinyl

HRID 536305Notes

Reaction equation

HRID 536305 reaction equation
Cl.Cl.[CH3:3][C@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[C@H:9]1[CH2:13][CH2:12][NH:11][CH2:10]1.Cl[C:15]1[CH:16]=[CH:17][C:18]([N+:21]([O-:23])=[O:22])=[N:19][CH:20]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH3:3][C@H:4]1[CH2:8][CH2:7][CH2:6][N:5]1[C@H:9]1[CH2:13][CH2:12][N:11]([C:15]2[CH:20]=[N:19][C:18]([N+:21]([O-:23])=[O:22])=[CH:17][CH:16]=2)[CH2:10]1

Participants

5

Conditions

Temperature
65 °C

Procedure

To a solution of (2S,3′S)-2-methyl-[1,3′]bipyrrolidinyl dihydrochloride (0.530 g, 2.35 mmol,) in acetonitrile (25 mL) was added 5-chloro-2-nitro-pyridine (0.561 g, 3.53 mmol,) and powdered potassium carbonate (1.30 g, 9.40 mmol). The reaction mixture was then heated to 65° C. for 4.0 hr, then at 45° C. for 16 hr. The reaction mixture was then allowed to cool to room temperature and filtered through a 10.0 g Varian Bond Elut SCX (stong cation-exchange) cartridge eluting with 50 mL of (1:1) methanol in dichloromethane, 25 mL of methanol, followed by 7N ammonia in methanol (50 mL). The filtrate was concentrated under vacuum to obtain a compound which was purified again by column chromatography on silica gel eluting with methanol in dichloromethane (0-10%) to afford 0.110 g (17%) of the title compound.

Workup

  1. temperatureto cool to room temperature
  2. filtrationfiltered through a 10.0 g Varian Bond Elut SCX (stong cation-exchange) cartridge
  3. washeluting with 50 mL of (1:1) methanol in dichloromethane, 25 mL of methanol
  4. concentrationThe filtrate was concentrated under vacuum
  5. customto obtain a compound which
  6. customwas purified again by column chromatography on silica gel eluting with methanol in dichloromethane (0-10%)

Sources & evidence

ORD record
ord-a05d7d5d81894767ba042ba9fb2e5816
Source dataset
uspto-grants-2014_10
Patent number
US08859588B2

Reaction notes

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