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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344415Generated: November 1, 2026

Acetaldehyde → HCID 54435522, compound

https://huagongshe.com/reaction/344415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 53862130HCID 53862130—
ProductHCID 54435522HCID 54435522—

Reaction Steps

4-Amino-5-chloro-2-methoxy-N-((1-(5-(4-methylbenzylamino)pentyl)-piperidin-4-yl)methyl)benzamide (1.5 g) as starting compound, acetaldehyde (0.22 ml) and sodium cyanoborohydride (0.25 g) were reacted and treated in the same manner as in Example 136 to give 0.7 g of 4-amino-5-chloro-N-((1-(5-(N-ethyl-N-(4-methylbenzyl)amino)pentyl)piperidin-4-yl)-methyl)-2-methoxybenzamide.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05864039
Source datasetuspto-grants-1999_01
ORD IDord-d13e3c4ca56944df9910a24c3d22c36e
Source noteuspto-grants-1999_01