Sodium borohydride → N-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamine

HRID 236734Notes

Reaction equation

HRID 236734 reaction equation
[C:1]1([CH2:7][N:8]2[CH2:13][CH2:12][C:11](=[N:14][C:15]3[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=3)[CH2:10][CH2:9]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[BH4-].[Na+]>C(O)C>[C:1]1([CH2:7][N:8]2[CH2:9][CH2:10][CH:11]([NH:14][C:15]3[CH:16]=[N:17][CH:18]=[CH:19][CH:20]=3)[CH2:12][CH2:13]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1

Participants

4

Reactant 2

HCID 4311764Sodium borohydrideHCID 10706822N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine

Product 1

HCID 10706957N-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamine

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Conditions

Temperature
50 °C

Procedure

To a stirred solution of 27 parts of N-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamine in 40 parts of ethanol are added portionwise 3.8 parts of sodium borohydride. After the addition is complete, the whole is heated to 50° C. The solvent is evaporated. The oily residue is dissolved in 150 parts of hydrochloric acid 1 N and filtered. The filtrate is rendered alkaline with ammonium hydroxide and extracted with methylbenzene. The organic layer is dried over magnesium sulfate, filtered and evaporated. The solid residue is washed with 2,2'-oxybispropane and dried, yielding 14 parts of N-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamine; mp. 131°-133° C.; beige, amorphous powder.

Workup

  1. additionAfter the addition
  2. customThe solvent is evaporated
  3. dissolutionThe oily residue is dissolved in 150 parts of hydrochloric acid 1 N
  4. filtrationfiltered
  5. extractionextracted with methylbenzene
  6. dry with materialThe organic layer is dried over magnesium sulfate
  7. filtrationfiltered
  8. customevaporated
  9. washThe solid residue is washed with 2,2'-oxybispropane
  10. customdried

Sources & evidence

ORD record
ord-d3bafbd3a7c1427bb4ec3c1c4d13b7bb
Source dataset
uspto-grants-1979_06
Patent number
US04157393

Reaction notes

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