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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1247113Generated: October 28, 2026

Methyl Ethyl Ketone → HCID 21906470, compound

https://huagongshe.com/reaction/1247113

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl Ethyl KetoneHCID 6569—
ReactantSodium cyanoborohydrideHCID 5003444—
Reactant5-Chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamideHCID 21906309—
SolventTetrahydrofuranHCID 8028—
SolventAcetic acid methanolHCID 10129899—
ProductHCID 21906470HCID 2190647050.1%

Reaction Conditions

Temperature50 °C

Reaction Steps

A solution of 5-chloro-N-(5-methylpyridin-2-yl)-2-[(4-piperidinylmethyl)amino]benzamide from Example 99-A (0.45 g, 1.25 mmol) in 10 mL of 95:5 methanol-acetic acid was treated with methylethyl ketone (1.12 mL, 12.5 mmol), followed by sodium cyanoborohydride (5.0 ml of a 1 M solution in tetrahydrofuran, 6.0 mmol). After stirring at 50° C. for 96 h, the mixture was concentrated in vacuo; and the residue was subjected to silica gel chromatography. Elution with 9:1 dichloromethane-methanol afforded 0.26 g (50%) of the title compound as a tan solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07129245B2
Source datasetuspto-grants-2006_10
ORD IDord-4e726bf6c3eb49d8a88ba81d5144969c
Source noteuspto-grants-2006_10