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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 28125Generated: October 29, 2026

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

https://huagongshe.com/reaction/28125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
ReactantN-[1-(phenylmethyl)-4-piperidinylidene]-3-pyridinamineHCID 10706822—
SolventEthanolHCID 702—
ProductN-[1-(phenylmethyl)-4-piperidinyl]-3-pyridinamineHCID 10706957—

Reaction Conditions

Temperature50 °C

Reaction Steps

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 IN 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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04225606
Source datasetuspto-grants-1980_09
ORD IDord-6ec1545350424b409648c95f9caadd8d
Source noteuspto-grants-1980_09