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Potassium hydride → Dihydro-6-diethoxyphosphinyl-1-pyrindine-6-sulfonic acid, ethyl ester

HRID 1290652
Notes
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Reaction equation

HRID 1290652 reaction equation
[H-].[K+].[CH2:3]([O:5][P:6]([CH2:11][S:12]([O:15][CH2:16][CH3:17])(=[O:14])=[O:13])([O:8][CH2:9][CH3:10])=[O:7])[CH3:4].Cl[CH2:19][C:20]1[C:25]([CH2:26]Cl)=[CH:24][CH:23]=[CH:22][N:21]=1>CS(C)=O>[CH2:3]([O:5][P:6]([O:8][CH2:9][CH3:10])([C:11]1([S:12]([O:15][CH2:16][CH3:17])(=[O:13])=[O:14])[CH:19]=[C:20]2[C:25]([CH:24]=[CH:23][CH2:22][NH:21]2)=[CH:26]1)=[O:7])[CH3:4]
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 3

HCID 82127Potassium hydrideHCID 10934205Ethyl (diethoxyphosphoryl)methanesulfonateHCID 145187502,3-Bis(chloromethyl)pyridine

Product 1

HCID 86752567Dihydro-6-diethoxyphosphinyl-1-pyrindine-6-sulfonic acid, ethyl ester

Reagents, catalysts & solvents 1

HCID 679Dimethyl SulfoxideSolvent2×

Conditions

Temperature
90 °C

Procedure

To an ice bath chilled solution of 35% potassium hydride in mineral oil (5.0 mmol) stirring under argon DMSO (7 ml) is added a solution of diethoxyphosphinyl methanesulfonic acid, ethyl ester (2.5 mmol) [prepared as described in J. C. Carretero, et. al., Tetrahedron, Vol. 43, pp. 5125-5134 (No. 21) 1987] in DMSO (5 ml). On completion of a dropwise addition, the resulting solution is stirred at room temperature for one hour. A solution of 2,3-bis(chloromethyl)pyridine (2.5 mmol) [prepared as described in K. Tsuda, et. al., Chem. Pharm. Bull., Vol.1, pp. 142, 1953] in DMSO (2 ml) is added slowly and the reaction mixture is then heated at 90° C. for 1 hour. After cooling, the reaction mixture is concentrated under reduced pressure and the desired product is purified by flash chromatography using a 5-15% isopropanol in methylene chloride gradient on silica gel.

Workup

  1. customprepared
  2. additionOn completion of a dropwise addition
  3. stirringthe resulting solution is stirred at room temperature for one hour
  4. temperatureAfter cooling
  5. concentrationthe reaction mixture is concentrated under reduced pressure
  6. customthe desired product is purified by flash chromatography

Sources & evidence

ORD record
ord-230599ab80d54575b37403df5149cc58
Source dataset
uspto-grants-1998_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US05753634

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes