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Ammonia → {(3S)-3-(3,4-Dichlorophenyl)-1-[6-(dimethylamino)-2-pyridinyl]-6-oxopiperidinyl}acetaldehyde Hydrochloride

HRID 1829174
Notes
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Reaction equation

HRID 1829174 reaction equation
[C:1](=[O:4])([O-])[O-].[K+].[K+].Br[C:8]1[N:13]=[C:12]([N:14]([CH3:16])[CH3:15])[CH:11]=[CH:10][CH:9]=1.[Cl:17][C:18]1[CH:19]=[C:20]([C@:25]2([CH2:32][CH:33]3OCCO3)CN[C:28](=[O:31])[CH2:27][CH2:26]2)[CH:21]=[CH:22][C:23]=1[Cl:24].[ClH:38].[NH3:39]>CN1CCCC1=O.[Cu]I>[ClH:17].[Cl:38][C:22]1[CH:21]=[C:20]([C@@H:25]2[CH2:26][CH2:27][C:28](=[O:31])[N:39]([C:8]3[CH:9]=[CH:10][CH:11]=[C:12]([N:14]([CH3:16])[CH3:15])[N:13]=3)[CH:32]2[CH2:33][CH:1]=[O:4])[CH:19]=[CH:18][C:23]=1[Cl:24]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

8

Reactant 5

HCID 222AmmoniaHCID 313Hydrochloric AcidHCID 11430Potassium CarbonateHCID 10882069(5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinoneHCID 140060626-bromo-N,N-dimethylpyridin-2-amine

Product 1

HCID 86593350
{(3S)-3-(3,4-Dichlorophenyl)-1-[6-(dimethylamino)-2-pyridinyl]-6-oxopiperidinyl}acetaldehyde Hydrochloride

Reagents, catalysts & solvents 2

HCID 24350Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)CatalystHCID 13387N-methyl-2-pyrrolidoneSolvent

Conditions

Temperature
140 °C

Procedure

Copper (I) iodide (6.4 g, 33.3 mmol), potassium carbonate (6.3 g, 45.4 mmol) and 6-bromo-2-(dimethylamino)pyridine (WO 9843971) (9 g, 45.4 mmol) were added consecutively to a solution of (5S)-5-(3,4-dichlorophenyl)-5-(1,3-dioxolan-2-ylmethyl)-2-piperidinone (WO 9807722) (10 g, 30.3 mmol), in 1-methyl-2-pyrrolidinone (50 ml), and the mixture was stirred at 140° C. for 4 hours. The cooled mixture was poured into 4N hydrochloric acid, then carefully basified using 10% aqueous ammonia. The aqueous mixture was extracted with ethyl acetate (3×200 ml), and the combined organic extracts were washed with brine, dried (MgSO4) and evaporated under reduced pressure to give an orange oil. The crude product was purified by column chromatography on silica gel using methanol:dichloromethane (5:95) as eluant, and repeated using ethyl acetate as eluant. The product was treated with 1N ethereal hydrochloric acid, and evaporated under reduced pressure to afford the title compound.

Workup

  1. extractionThe aqueous mixture was extracted with ethyl acetate (3×200 ml)
  2. washthe combined organic extracts were washed with brine
  3. dry with materialdried (MgSO4)
  4. customevaporated under reduced pressure
  5. customto give an orange oil
  6. customThe crude product was purified by column chromatography on silica gel
  7. additionThe product was treated with 1N ethereal hydrochloric acid
  8. customevaporated under reduced pressure

Sources & evidence

ORD record
ord-21c838b827c04abdbed331dd02a294dc
Source dataset
uspto-grants-2006_06
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07060836B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes