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HCID 22266530, compound → 1-butyl-3-hydroxy-4(N,N-dimethylaminomethyl)pyridine-2-thione

HRID 416564
Notes
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Reaction equation

HRID 416564 reaction equation
[CH2:1]([N:5]1[CH:10]=[CH:9][CH:8]=[C:7]([OH:11])[C:6]1=[S:12])[CH2:2][CH2:3][CH3:4]>C(O)C>[CH2:1]([N:5]1[CH:10]=[CH:9][C:8]([CH2:1][N:5]([CH3:10])[CH3:6])=[C:7]([OH:11])[C:6]1=[S:12])[CH2:2][CH2:3][CH3:4]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

3

Reactant 1

HCID 22266530HCID 22266530, compound

Product 1

HCID 222665191-butyl-3-hydroxy-4(N,N-dimethylaminomethyl)pyridine-2-thioneYield 198.2%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
75 °C

Procedure

To a solution of 1-butyl-3-hydroxypyridine-2-thione (2-034-04) (1.0 g) in ethanol containing 10% water (20 mL) was added N, N, N′, N′-teteramethyldiaminomethane (1.70 g) at room temperature. After the reaction mixture was stirred at 75° C. for 24 h, the solvent was evaporated under reduced pressure to give 1-butyl-3-hydroxy-4(N,N-dimethylaminomethyl)pyridine-2-thione (2-034-05) (1.3 g, 95%) as an oil.

Workup

  1. customthe solvent was evaporated under reduced pressure

Sources & evidence

ORD record
ord-d192df92636240e1a22cd6a213a9c0d9
Source dataset
uspto-grants-2012_01
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08088924B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes