HCID 22258740, compound → HCID 22258804, compound

HRID 1767361Notes

Reaction equation

HRID 1767361 reaction equation
[NH2:1][C:2]1[C:7]([CH2:8][OH:9])=[C:6]([CH:10]2[CH2:15][CH2:14][CH2:13][N:12]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH2:11]2)[CH:5]=[C:4]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[O:29][CH2:30][C:31]2[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=2)[N:3]=1>C(Cl)Cl.[O-2].[Mn+4].[O-2]>[NH2:1][C:2]1[C:7]([CH:8]=[O:9])=[C:6]([CH:10]2[CH2:15][CH2:14][CH2:13][N:12]([C:16]([O:18][C:19]([CH3:22])([CH3:21])[CH3:20])=[O:17])[CH2:11]2)[CH:5]=[C:4]([C:23]2[CH:28]=[CH:27][CH:26]=[CH:25][C:24]=2[O:29][CH2:30][C:31]2[CH:32]=[CH:33][CH:34]=[CH:35][CH:36]=2)[N:3]=1

Participants

4

Reactant 1

HCID 22258740HCID 22258740, compound

Product 1

HCID 22258804HCID 22258804, compoundYield 73%

Reagents, catalysts & solvents 2

HCID 178418406HCID 178418406, compoundCatalystHCID 6344DichloromethaneSolvent

Procedure

To a solution of tert-butyl 3-[2-amino-6-[2-(benzyloxy)phenyl]-3-(hydroxy-methyl)-4-pyridinyl]-1-piperidinecarboxylate (0.900 g, 1.838 mmol) in methylene chloride (20 mL) was added manganese (IV) oxide (3.20 g, 36.8 mmol). After stirred at room temperature for 40 min, the mixture was filtered to remove the manganese salt. The filtrate was concentrated under reduced pressure. The resulting solid was purified by recrystallization from a mixture of ethyl acetate and hexane to give tert-butyl 3-[2-amino-6-[2-(benzyloxy)phenyl]-3-formyl-4-pyridinyl]-1-piperidine-carboxylate. (0.651 g, yield; 73%)

Workup

  1. filtrationthe mixture was filtered
  2. customto remove the manganese salt
  3. concentrationThe filtrate was concentrated under reduced pressure
  4. customThe resulting solid was purified by recrystallization from a mixture of ethyl acetate and hexane

Sources & evidence

ORD record
ord-de89dcea70a74dbf896dfcc4d1cb7423
Source dataset
uspto-grants-2007_06
Patent number
US07232909B2

Reaction notes

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