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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 344423Generated: October 31, 2026

Acetaldehyde → HCID 53773943, compound

https://huagongshe.com/reaction/344423

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetaldehydeHCID 177—
ReactantSodium cyanoborohydrideHCID 5003444—
ReactantHCID 54465414HCID 54465414—
ProductHCID 53773943HCID 53773943—

Reaction Steps

4-Amino-5-chloro-2-methoxy-N-((1-(5-(2-naphthylmethylamino)pentyl)-piperidin-4-yl)methyl)benzamide (1.50 g) as starting compound, acetaldehyde (0.18 ml) and sodium cyanoborohydride (0.40 g) were reacted and treated in the same manner as in Example 136 to give 1.1 g of 4-amino-5-chloro-N-((1-(5-(N-ethyl-N-(2-naphthylmethyl)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-c3d14214f7c64e34a53ded3b48fc3461
Source noteuspto-grants-1999_01