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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1377573Generated: October 30, 2026

Sodium borohydride → 6,11-DIHYDRO-11-(4-PIPERIDINYL)-5H-BENZO[5,6]CYCLOHEPTA[1,2-b]PYRIDINE

https://huagongshe.com/reaction/1377573

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium borohydrideHCID 4311764—
Reactant(1-Methylpiperidin-4-yl)[3-(2-phenylethyl)pyridin-2-yl]methanoneHCID 14885588—
SolventMethanolHCID 887—
SolventWaterHCID 962—
Product6,11-DIHYDRO-11-(4-PIPERIDINYL)-5H-BENZO[5,6]CYCLOHEPTA[1,2-b]PYRIDINEHCID 1068401897.6%

Reaction Steps

To a mixture of 5.0 g (16.2 mmole) of (1-methyl-4-piperidinyl) [3-(2-phenylethyl)-2-pyridinyl]methanone (which can be prepared in the same manner as described in Preparative Example 1, Steps A-D) in 70 mL of methanol was added portionwise 0.8 g (21.1 mmole) of sodium borohydride. The next day the solution was concentrated in vacuo to give a slurry which was dissolved in water and extracted with CHCl3. The combined organic portions were dried over MgSO4, filtered, and concentrated in vacuo to provide a liquid which was distilled (bp 190°-195° C. 1 mm Hg) to give 4.4 gms of the title compound as a viscous oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05665726
Source datasetuspto-grants-1997_09
ORD IDord-3ed45a8f3144400cb2f79868d3e8c6a7
Source noteuspto-grants-1997_09